A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690743



Internal ID15080709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31396930..31496186hg38UCSC Ensembl
Innerchr6:31364707..31463963hg19UCSC Ensembl
Innerchr6:31472686..31571942hg18UCSC Ensembl
Innerchr6:31472686..31571942hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3899257
hg1999257
hg1899257
hg1799257
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690743
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