A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687714



Internal ID15424366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69424292..69438084hg38UCSC Ensembl
Innerchr17:67420433..67434225hg19UCSC Ensembl
Innerchr17:64932028..64945820hg18UCSC Ensembl
Innerchr17:64932028..64945820hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3813793
hg1913793
hg1813793
hg1713793
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520649
Supporting Variants
Samples
Known GenesMAP2K6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687714
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