A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156370



Internal ID15878979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75531228..75564634hg38UCSC Ensembl
Innerchr8:76443463..76476869hg19UCSC Ensembl
Innerchr8:76606018..76639424hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3833407
hg1933407
hg1833407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611562
Supporting Variants
SamplesHGDP01286
Known GenesHNF4G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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