A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573868



Internal ID16014591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:169598..171764hg38UCSC Ensembl
Innerchr17:19389..21555hg19UCSC Ensembl
Innerchr17:19389..21555hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382167
hg192167
hg182167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5348n54
Supporting Variantsnssv864088, nssv864087
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573868
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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