A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524499



Internal ID15451792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56893880..56899561hg38UCSC Ensembl
Innerchr17:54971241..54976922hg19UCSC Ensembl
Innerchr17:52326240..52331921hg18UCSC Ensembl
Innerchr17:52326240..52331921hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg385682
hg195682
hg185682
hg175682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700441
Samples
Known GenesTRIM25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524499
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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