A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034360



Internal ID15887546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64399736..64405443hg38UCSC Ensembl
Innerchr5:63695563..63701270hg19UCSC Ensembl
Innerchr5:63731319..63737026hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385708
hg195708
hg185708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598358
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1034360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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