A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173347



Internal ID15877415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:171412607..171440376hg38UCSC Ensembl
Innerchr1:171381746..171409515hg19UCSC Ensembl
Innerchr1:169648370..169676139hg18UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3827770
hg1927770
hg1827770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548189
Supporting Variants
SamplesHGDP00984
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173347
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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