A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031795



Internal ID18774329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98093498..98120427hg38UCSC Ensembl
Innerchr8:99105726..99132655hg19UCSC Ensembl
Innerchr8:99174902..99201831hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3826930
hg1926930
hg1826930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757326
Samples
Known GenesC8orf47, HRSP12, POP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031795
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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