A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605701



Internal ID16046424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:889622..890429hg38UCSC Ensembl
Innerchr7:929259..930066hg19UCSC Ensembl
Innerchr7:895785..896592hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38808
hg19808
hg18808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077809
Samples
Known GenesGET4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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