A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522189



Internal ID15449482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10900096..10905496hg38UCSC Ensembl
Innerchr17:10803413..10808813hg19UCSC Ensembl
Innerchr17:10744138..10749538hg18UCSC Ensembl
Innerchr17:10744138..10749538hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385401
hg195401
hg185401
hg175401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694964
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522189
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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