A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527258



Internal ID15454551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:44572414..44578375hg38UCSC Ensembl
Innerchr17:42649782..42655743hg19UCSC Ensembl
Innerchr17:40005308..40011269hg18UCSC Ensembl
Innerchr17:40005308..40011269hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385962
hg195962
hg185962
hg175962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703663
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527258
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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