A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv994n54



Internal ID22768889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20553102..20588852hg38UCSC Ensembl
chr10:20842031..20877781hg19UCSC Ensembl
chr10:20882037..20917787hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3835751
hg1935751
hg1835751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550166, nsv550179
SamplesNINDS_84
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv994n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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