A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1042049



Internal ID15895235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135946278..135961861hg38UCSC Ensembl
Innerchr5:135281967..135297550hg19UCSC Ensembl
Innerchr5:135309866..135325449hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3815584
hg1915584
hg1815584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599796
Supporting Variants
Samples
Known GenesLECT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1042049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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