A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611806



Internal ID16052529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98076023..98105304hg38UCSC Ensembl
Innerchr8:99088251..99117532hg19UCSC Ensembl
Innerchr8:99157427..99186708hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3829282
hg1929282
hg1829282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156140
SamplesHGDP01053
Known GenesC8orf47, HRSP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611806
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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