A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528790



Internal ID15456083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78291626..78309532hg38UCSC Ensembl
Innerchr17:76287707..76305613hg19UCSC Ensembl
Innerchr17:73799302..73817208hg18UCSC Ensembl
Innerchr17:73799302..73817208hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3817907
hg1917907
hg1817907
hg1717907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705460
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528790
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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