A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1024069



Internal ID16318025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8703036..8748515hg38UCSC Ensembl
Innerchr5:8703148..8748627hg19UCSC Ensembl
Innerchr5:8756148..8801627hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3845480
hg1945480
hg1845480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597048
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)nssv1024069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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