A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152998



Internal ID15877263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8526974..8539701hg38UCSC Ensembl
Innerchr5:8527086..8539813hg19UCSC Ensembl
Innerchr5:8580086..8592813hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3812728
hg1912728
hg1812728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597029
Supporting Variants
SamplesHGDP00958
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152998
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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