A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695626



Internal ID15085592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94215510..94219562hg38UCSC Ensembl
Innerchr6:94925228..94929280hg19UCSC Ensembl
Innerchr6:94981949..94986001hg18UCSC Ensembl
Innerchr6:94981949..94986001hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg384053
hg194053
hg184053
hg174053
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695626
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