A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019021



Internal ID18761554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12270819..12335890hg38UCSC Ensembl
Innerchr7:12310445..12375516hg19UCSC Ensembl
Innerchr7:12276970..12342041hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3865072
hg1965072
hg1865072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642962
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)nsv1019021
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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