A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029941



Internal ID18772472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12311969..12404864hg38UCSC Ensembl
Innerchr7:12351595..12444490hg19UCSC Ensembl
Innerchr7:12318120..12411015hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3892896
hg1992896
hg1892896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6272n100
Supporting Variantsnssv3642963
Samples
Known GenesVWDE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029941
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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