A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520626



Internal ID15101233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155454197..155465199hg38UCSC Ensembl
Innerchr7:155246892..155257894hg19UCSC Ensembl
Innerchr7:154939653..154950655hg18UCSC Ensembl
Innerchr7:154746368..154757370hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3811003
hg1911003
hg1811003
hg1711003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673323, nssv691888, nssv697992
Samples
Known GenesEN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520626
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer