A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703598



Internal ID15440250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62100143..62104422hg38UCSC Ensembl
Innerchr17:60177504..60181783hg19UCSC Ensembl
Innerchr17:57532286..57536565hg18UCSC Ensembl
Innerchr17:57532286..57536565hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg384280
hg194280
hg184280
hg174280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527199
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703598
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