A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696998



Internal ID15086964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:37399310..37400742hg38UCSC Ensembl
Innerchr1:37864911..37866343hg19UCSC Ensembl
Innerchr1:37637498..37638930hg18UCSC Ensembl
Innerchr1:37534004..37535436hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381433
hg191433
hg181433
hg171433
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519697
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696998
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