A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028921



Internal ID19118140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61692688hg38UCSC Ensembl
Innerchr9:44727847..44900526hg19UCSC Ensembl
Innerchr9:44667843..44840522hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38172680
hg19172680
hg18172680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7603n100
Supporting Variantsnssv3695558, nssv3695557
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)nsv1028921
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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