A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015581



Internal ID18758115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14083382..14159376hg38UCSC Ensembl
Innerchr7:14123007..14199001hg19UCSC Ensembl
Innerchr7:14089532..14165526hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3875995
hg1975995
hg1875995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752895
Samples
Known GenesDGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015581
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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