A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020620



Internal ID19109839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61600636hg38UCSC Ensembl
Innerchr9:44727847..44808474hg19UCSC Ensembl
Innerchr9:44667843..44748470hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3880628
hg1980628
hg1880628
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7601n100
Supporting Variantsnssv3757607, nssv3693085, nssv3693097, nssv3693081, nssv3693122, nssv3693121, nssv3693117, nssv3693094, nssv3693096, nssv3757609, nssv3693107, nssv3693116, nssv3693105, nssv3757614, nssv3693103, nssv3693098, nssv3693125, nssv3693091, nssv3693083, nssv3691969, nssv3693101, nssv3693090, nssv3693084, nssv3693108, nssv3693099, nssv3693113, nssv3693119, nssv3693127, nssv3693109, nssv3693102, nssv3693089, nssv3693106, nssv3693095, nssv3757613, nssv3693104, nssv3693114, nssv3693088, nssv3693126, nssv3693080, nssv3693087, nssv3693100, nssv3693124, nssv3691966, nssv3757611, nssv3693115, nssv3691970, nssv3757606, nssv3691967, nssv3693128, nssv3693110, nssv3693129, nssv3693086, nssv3691968, nssv3757610, nssv3693118, nssv3757615, nssv3693111, nssv3693130, nssv3693079, nssv3693131, nssv3757608, nssv3757612, nssv3693078, nssv3693123, nssv3693093, nssv3693112, nssv3693092, nssv3693082, nssv3693120
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020620
Frequency
Sample Size11257
Observed Gain40
Observed Loss29
Observed Complex0
Frequencyn/a


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