A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669281



Internal ID15059247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50134964..50136764hg38UCSC Ensembl
Innerchr3:50172397..50174197hg19UCSC Ensembl
Innerchr3:50147401..50149201hg18UCSC Ensembl
Innerchr3:50147401..50149201hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381801
hg191801
hg181801
hg171801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515986
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669281
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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