A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701624



Internal ID15438276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137580306..137583210hg38UCSC Ensembl
Innerchr6:137901443..137904347hg19UCSC Ensembl
Innerchr6:137943136..137946040hg18UCSC Ensembl
Innerchr6:137943136..137946040hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382905
hg192905
hg182905
hg172905
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525493
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701624
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