A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015951



Internal ID19105169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8839730..8994040hg38UCSC Ensembl
Innerchr7:8879360..9033670hg19UCSC Ensembl
Innerchr7:8845885..9000195hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38154311
hg19154311
hg18154311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6258n100
Supporting Variantsnssv3642856
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)nsv1015951
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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