A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527475



Internal ID15108082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8140435..8189376hg38UCSC Ensembl
Innerchr17:8043753..8092694hg19UCSC Ensembl
Innerchr17:7984478..8033419hg18UCSC Ensembl
Innerchr17:7984478..8033419hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3848942
hg1948942
hg1848942
hg1748942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703919
Samples
Known GenesC17orf59, MIR4521, MIR6883, PER1, TMEM107, VAMP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527475
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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