A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523707



Internal ID15451000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153193876..153195547hg38UCSC Ensembl
Innerchr6:153515011..153516682hg19UCSC Ensembl
Innerchr6:153556704..153558375hg18UCSC Ensembl
Innerchr6:153607125..153608796hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381672
hg191672
hg181672
hg171672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699516
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523707
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