A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638243



Internal ID6678341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24132538..24136921hg38UCSC Ensembl
Innerchr16:24132548..24136911hg38UCSC Ensembl
Outerchr16:24132528..24136931hg38UCSC Ensembl
chr16:24143859..24148242hg19UCSC Ensembl
Innerchr16:24143869..24148232hg19UCSC Ensembl
Outerchr16:24143849..24148252hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384384
hg194384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15429929
SamplesNA18517
Known GenesPRKCB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638243
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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