A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643427



Internal ID18595022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38240623..38284089hg38UCSC Ensembl
Innerchr7:38280224..38323690hg19UCSC Ensembl
Innerchr7:38246749..38290215hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3843467
hg1943467
hg1843467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026846
Supporting Variants
Samples
Known GenesTARP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643427
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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