A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661909



Internal ID15051875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71115426..71124357hg38UCSC Ensembl
Innerchr2:71342556..71351487hg19UCSC Ensembl
Innerchr2:71196064..71204995hg18UCSC Ensembl
Innerchr2:71254211..71263142hg17UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg388932
hg198932
hg188932
hg178932
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517762
Supporting Variants
Samples
Known GenesMCEE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661909
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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