A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153001



Internal ID15879967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702260..8746994hg38UCSC Ensembl
Innerchr5:8702372..8747106hg19UCSC Ensembl
Innerchr5:8755372..8800106hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844735
hg1944735
hg1844735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597033
Supporting Variants
SamplesNINDS_132
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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