A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674089



Internal ID15064055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1635252..1638896hg38UCSC Ensembl
Innerchr17:1538546..1542190hg19UCSC Ensembl
Innerchr17:1485296..1488940hg18UCSC Ensembl
Innerchr17:1485296..1488940hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383645
hg193645
hg183645
hg173645
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516055
Supporting Variants
Samples
Known GenesSCARF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674089
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