A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639081



Internal ID7025864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75036890..75056954hg38UCSC Ensembl
chr16:75070788..75090852hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3820065
hg1920065
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15520442, essv15520443
SamplesHG01791, HG01148
Known GenesZNRF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639081
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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