A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682227



Internal ID15072193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1708905..1748486hg38UCSC Ensembl
Innerchr17:1612199..1651780hg19UCSC Ensembl
Innerchr17:1558949..1598530hg18UCSC Ensembl
Innerchr17:1558949..1598530hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3839582
hg1939582
hg1839582
hg1739582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516886
Supporting Variants
Samples
Known GenesMIR22, MIR22HG, SERPINF2, TLCD2, WDR81
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682227
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