A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524211



Internal ID8418486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3214108..3268761hg38UCSC Ensembl
Innerchr4:3215835..3270488hg19UCSC Ensembl
Innerchr4:3185633..3240286hg18UCSC Ensembl
Innerchr4:3252838..3307457hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3854654
hg1954654
hg1854654
hg1754620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700098
Samples
Known GenesHTT, MSANTD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524211
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