A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585176



Internal ID16372585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:602943..625293hg38UCSC Ensembl
Innerchr20:583587..605937hg19UCSC Ensembl
Innerchr20:531587..553937hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3822351
hg1922351
hg1822351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150943
SamplesNINDS_23
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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