A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1172581



Internal ID15879361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2249085..2289210hg38UCSC Ensembl
Innerchr1:2180524..2220649hg19UCSC Ensembl
Innerchr1:2170384..2210509hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3840126
hg1940126
hg1840126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545068
Supporting Variants
SamplesHGDP01351
Known GenesSKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1172581
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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