A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526205



Internal ID15453498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45177344..45177910hg38UCSC Ensembl
Innerchr2:45404483..45405049hg19UCSC Ensembl
Innerchr2:45257987..45258553hg18UCSC Ensembl
Innerchr2:45316134..45316700hg17UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38567
hg19567
hg18567
hg17567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702468
Samples
Known GenesLINC01121
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526205
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