A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608057



Internal ID16048780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102799737..102898068hg38UCSC Ensembl
Innerchr7:102440184..102538515hg19UCSC Ensembl
Innerchr7:102227420..102325751hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3898332
hg1998332
hg1898332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156559
SamplesHGDP00609
Known GenesFAM185A, FBXL13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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