A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152448



Internal ID15532704
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
SamplesHGDP01357
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152448
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer