A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153977



Internal ID15873100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103908939..103929286hg38UCSC Ensembl
Innerchr5:103244640..103264987hg19UCSC Ensembl
Innerchr5:103272539..103292886hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3820348
hg1920348
hg1820348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599199
Supporting Variants
SamplesHGDP00124
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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