A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107311



Internal ID15960497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17483518..17505730hg38UCSC Ensembl
Innerchr8:17341027..17363239hg19UCSC Ensembl
Innerchr8:17385392..17407618hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3822213
hg1922213
hg1822227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610680
Supporting Variants
Samples
Known GenesSLC7A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107311
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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