A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026925



Internal ID19116143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756249..97773151hg38UCSC Ensembl
Innerchr7:97385561..97402463hg19UCSC Ensembl
Innerchr7:97223497..97240399hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3816903
hg1916903
hg1816903
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655265, nssv3655263, nssv3655260, nssv3655255, nssv3655271, nssv3655266, nssv3755445, nssv3655259, nssv3755440, nssv3655269, nssv3655264, nssv3655270, nssv3755444, nssv3655256, nssv3655257, nssv3755439, nssv3655267, nssv3755438, nssv3655261, nssv3755442, nssv3755443, nssv3655268, nssv3655258, nssv3655262, nssv3655272, nssv3755441
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)nsv1026925
Frequency
Sample Size11257
Observed Gain5
Observed Loss21
Observed Complex0
Frequencyn/a


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