A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173798



Internal ID15508332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22125352..22186354hg38UCSC Ensembl
Innerchr1:22451845..22512847hg19UCSC Ensembl
Innerchr1:22324432..22385434hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3861003
hg1961003
hg1861003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545747
Supporting Variants
Samples1780862415_A
Known GenesWNT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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