A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574338



Internal ID16361747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8746398..8747107hg38UCSC Ensembl
Innerchr17:8649716..8650425hg19UCSC Ensembl
Innerchr17:8590441..8591150hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38710
hg19710
hg18710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866757
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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