A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153409



Internal ID15880233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164234098..164287024hg38UCSC Ensembl
Innerchr3:163951886..164004812hg19UCSC Ensembl
Innerchr3:165434580..165487506hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3852927
hg1952927
hg1852927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592439
Supporting Variants
SamplesNINDS_178
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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