A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755437



Internal ID19053718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97743281..97774916hg38UCSC Ensembl
Innerchr7:97372593..97404228hg19UCSC Ensembl
Innerchr7:97210529..97242164hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3831636
hg1931636
hg1831636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022849
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)nssv3755437
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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