A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674706



Internal ID18626301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156928636..156956417hg38UCSC Ensembl
Innerchr7:156721330..156749111hg19UCSC Ensembl
Innerchr7:156414091..156441872hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3827782
hg1927782
hg1827782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015433
Supporting Variants
Samples
Known GenesNOM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674706
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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