A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574334



Internal ID16015057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8096271..8110990hg38UCSC Ensembl
Innerchr17:7999589..8014308hg19UCSC Ensembl
Innerchr17:7940314..7955033hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3814720
hg1914720
hg1814720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866755
Samples
Known GenesALOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574334
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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