A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574098



Internal ID16361507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:860832..894127hg38UCSC Ensembl
Innerchr17:764072..797367hg19UCSC Ensembl
Innerchr17:710822..744117hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3833296
hg1933296
hg1833296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv865844
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574098
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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