A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574766



Internal ID16362175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36116419..36154629hg38UCSC Ensembl
Innerchr17:34443811..34482009hg19UCSC Ensembl
Innerchr17:31467924..31506122hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3838211
hg1938199
hg1838199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5535n54
Supporting Variantsnssv869890
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574766
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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