A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698224



Internal ID15434876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:173870366..173873684hg38UCSC Ensembl
Innerchr5:173297369..173300687hg19UCSC Ensembl
Innerchr5:173229975..173233293hg18UCSC Ensembl
Innerchr5:173229975..173233293hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg383319
hg193319
hg183319
hg173319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521607
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698224
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