A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695099



Internal ID15085065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46615069..46628595hg38UCSC Ensembl
Innerchr1:47080741..47094267hg19UCSC Ensembl
Innerchr1:46853328..46866854hg18UCSC Ensembl
Innerchr1:46792761..46806287hg17UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3813527
hg1913527
hg1813527
hg1713527
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522319
Supporting Variants
Samples
Known GenesMOB3C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695099
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