A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576074



Internal ID16363483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77221926..77254393hg38UCSC Ensembl
Innerchr17:75218008..75250475hg19UCSC Ensembl
Innerchr17:72729603..72762070hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3832468
hg1932468
hg1832468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149812
SamplesHGDP00909
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576074
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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