A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525424



Internal ID15452717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54755970..54827165hg38UCSC Ensembl
Innerchr17:52833331..52904526hg19UCSC Ensembl
Innerchr17:50188330..50259525hg18UCSC Ensembl
Innerchr17:50188330..50259525hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3871196
hg1971196
hg1871196
hg1771196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv180n21
Supporting Variantsnssv701548
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525424
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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