A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152997



Internal ID15532350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8467787..8664635hg38UCSC Ensembl
Innerchr5:8467900..8664747hg19UCSC Ensembl
Innerchr5:8520900..8717747hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38196849
hg19196848
hg18196848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597028
Supporting Variants
SamplesHGDP01297
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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