A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026846



Internal ID18769377
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 StatusM
Merged Variantsdgv6322n100
Supporting Variantsnssv3643427
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)nsv1026846
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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