A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863627



Internal ID3865443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74564188..74567585hg38UCSC Ensembl
chr10:76323946..76327343hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383398
hg193398
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623832
Supporting Variants
SamplesHG01342
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863627
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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