A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574318



Internal ID16361727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6394622..6416464hg38UCSC Ensembl
Innerchr17:6297942..6319784hg19UCSC Ensembl
Innerchr17:6238666..6260508hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3821843
hg1921843
hg1821843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866667
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574318
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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