A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612335



Internal ID16053058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134581482..134599122hg38UCSC Ensembl
Innerchr8:135593725..135611365hg19UCSC Ensembl
Innerchr8:135662907..135680547hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3817641
hg1917641
hg1817641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156648
SamplesHGDP00996
Known GenesZFAT, ZFAT-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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