A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528485



Internal ID15455778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121106155..121123158hg38UCSC Ensembl
Innerchr7:120746209..120763212hg19UCSC Ensembl
Innerchr7:120533445..120550448hg18UCSC Ensembl
Innerchr7:120340160..120357163hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3817004
hg1917004
hg1817004
hg1717004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705088
Samples
Known GenesCPED1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528485
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