A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022652



Internal ID19111870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101473041hg38UCSC Ensembl
Innerchr7:100968363..101116322hg19UCSC Ensembl
Innerchr7:100755083..100903042hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38147960
hg19147960
hg18147960
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3655325, nssv3655324
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022652
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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