A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023929



Internal ID16317885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702973..8744445hg38UCSC Ensembl
Innerchr5:8703085..8744557hg19UCSC Ensembl
Innerchr5:8756085..8797557hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3841473
hg1941473
hg1841473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597036
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1023929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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