A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156559



Internal ID15528239
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 StatusS
Merged Variantsnsv608057
Supporting Variants
SamplesHGDP00609
Known GenesFAM185A, FBXL13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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