A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526290



Internal ID15106897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19710044..19748169hg38UCSC Ensembl
Innerchr17:19613357..19651482hg19UCSC Ensembl
Innerchr17:19553949..19592074hg18UCSC Ensembl
Innerchr17:19553949..19592074hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3838126
hg1938126
hg1838126
hg1738126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702571
Samples
Known GenesALDH3A1, SLC47A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526290
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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