A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156345



Internal ID15530914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17335502..17351024hg38UCSC Ensembl
Innerchr8:17193011..17208533hg19UCSC Ensembl
Innerchr8:17237382..17252904hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815523
hg1915523
hg1815523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610676
Supporting Variants
SamplesHGDP01012
Known GenesMTMR7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156345
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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