A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034202



Internal ID15887388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61331130..61341001hg38UCSC Ensembl
Innerchr5:60626957..60636828hg19UCSC Ensembl
Innerchr5:60662714..60672585hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg389872
hg199872
hg189872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598319
Supporting Variants
Samples
Known GenesZSWIM6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1034202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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