A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152449



Internal ID15534278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046892..4059672hg38UCSC Ensembl
Innerchr3:4088576..4101356hg19UCSC Ensembl
Innerchr3:4063576..4076356hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3812781
hg1912781
hg1812781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589416
Supporting Variants
SamplesNINDS_51
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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