A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025757



Internal ID19114974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126403590..126423377hg38UCSC Ensembl
Innerchr7:126043644..126063431hg19UCSC Ensembl
Innerchr7:125830880..125850667hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3819788
hg1919788
hg1819788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6614n100
Supporting Variantsnssv3662169
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)nsv1025757
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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