A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15270949



Internal ID5272765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63164722..63200612hg38UCSC Ensembl
chr15:63456921..63492811hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3835891
hg1935891
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636713
Supporting Variants
SamplesNA19225
Known GenesRAB8B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15270949
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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