A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094523



Internal ID15601023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131506702..131562661hg38UCSC Ensembl
Innerchr7:131191461..131247420hg19UCSC Ensembl
Innerchr7:130842001..130897960hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3855960
hg1955960
hg1855960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608424
Supporting Variants
Samples
Known GenesPODXL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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