A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608060



Internal ID16395469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102845807..102983745hg38UCSC Ensembl
Innerchr7:102486254..102624192hg19UCSC Ensembl
Innerchr7:102273490..102411428hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38137939
hg19137939
hg18137939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156560
SamplesHGDP00736
Known GenesFBXL13, LRRC17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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