A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025582



Internal ID19114800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56718140..56800076hg38UCSC Ensembl
Innerchr7:56785833..56867769hg19UCSC Ensembl
Innerchr7:56753327..56835263hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3881937
hg1981937
hg1881937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6365n100
Supporting Variantsnssv3661430, nssv3661431
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)nsv1025582
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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