A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610036



Internal ID16050759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7337975..7356455hg38UCSC Ensembl
Innerchr8:7195497..7213977hg19UCSC Ensembl
Innerchr8:7182907..7201387hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818481
hg1918481
hg1818481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105708
Samples
Known GenesFAM66B, USP17L4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610036
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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