A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1039823



Internal ID15893009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106894481..106897877hg38UCSC Ensembl
Innerchr5:106230182..106233578hg19UCSC Ensembl
Innerchr5:106258081..106261477hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg383397
hg193397
hg183397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599319
Supporting Variants
Samples
Known GenesLOC102467213
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1039823
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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