A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1025208



Internal ID15972478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10273860..10278491hg38UCSC Ensembl
Innerchr5:10273972..10278603hg19UCSC Ensembl
Innerchr5:10326972..10331603hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg384632
hg194632
hg184632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597118
Supporting Variants
Samples
Known GenesCMBL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1025208
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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