A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1024090



Internal ID16318046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8703036..8757578hg38UCSC Ensembl
Innerchr5:8703148..8757690hg19UCSC Ensembl
Innerchr5:8756148..8810690hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3854543
hg1954543
hg1854543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597050
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)nssv1024090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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