A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4914n54



Internal ID20138338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13200753..13206350hg38UCSC Ensembl
chr16:13294610..13300207hg19UCSC Ensembl
chr16:13202111..13207708hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385598
hg195598
hg185598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571490, nsv571493
Samples
Known GenesSHISA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4914n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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