A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3676683



Internal ID18974964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142451137..142491573hg38UCSC Ensembl
Innerchr7:142140374..142180826hg19UCSC Ensembl
Innerchr7:141819602..141860046hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3840437
hg1940453
hg1840445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015404
Supporting Variants
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)nssv3676683
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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