A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023151



Internal ID19112368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61598565hg38UCSC Ensembl
Innerchr9:44727847..44806403hg19UCSC Ensembl
Innerchr9:44667843..44746399hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3878557
hg1978557
hg1878557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7599n100
Supporting Variantsnssv3691961, nssv3757605, nssv3691957, nssv3691960, nssv3691964, nssv3691956, nssv3691959, nssv3691965, nssv3691963, nssv3691962, nssv3691958
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)nsv1023151
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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