A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638937



Internal ID7025722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69853067..69861167hg38UCSC Ensembl
Innerchr16:69853067..69861167hg38UCSC Ensembl
Outerchr16:69852881..69861220hg38UCSC Ensembl
chr16:69886970..69895070hg19UCSC Ensembl
Innerchr16:69886970..69895070hg19UCSC Ensembl
Outerchr16:69886784..69895123hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388101
hg198101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15503815
SamplesHG03439
Known GenesWWP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638937
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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