A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030799



Internal ID19120018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61619207hg38UCSC Ensembl
Innerchr9:44727847..44827045hg19UCSC Ensembl
Innerchr9:44667843..44767041hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3899199
hg1999199
hg1899199
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7601n100
Supporting Variantsnssv3692118, nssv3692127, nssv3692130, nssv3692128, nssv3760849, nssv3692124, nssv3760850, nssv3692136, nssv3692125, nssv3692131, nssv3692126, nssv3692129, nssv3692122, nssv3692139, nssv3692123, nssv3692119, nssv3760848, nssv3692132, nssv3692121, nssv3692138, nssv3692137, nssv3692133, nssv3692134, nssv3692140, nssv3692120, nssv3692135
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)nsv1030799
Frequency
Sample Size11257
Observed Gain24
Observed Loss2
Observed Complex0
Frequencyn/a


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