A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515649



Internal ID15443260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:161639883..161659888hg38UCSC Ensembl
Innerchr5:161066889..161086894hg19UCSC Ensembl
Innerchr5:160999467..161019472hg18UCSC Ensembl
Innerchr5:160999467..161019472hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3820006
hg1920006
hg1820006
hg1720006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662454, nssv657116, nssv675889, nssv680922, nssv693703, nssv666160, nssv690108, nssv663291, nssv684701, nssv654650, nssv675237, nssv659473, nssv679479, nssv655567, nssv664238
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515649
Frequency
Sample Size2026
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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