A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605702



Internal ID16046425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:890175..947983hg38UCSC Ensembl
Innerchr7:929812..987619hg19UCSC Ensembl
Innerchr7:896338..954145hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3857809
hg1957808
hg1857808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077810
Samples
Known GenesADAP1, GET4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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