A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623832



Internal ID6663999
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863627, essv13863630, essv13863631, essv13863633, essv13863632, essv13863629, essv13863628
SamplesHG01342, HG02703, NA18973, HG04141, NA20348, HG02545, HG01522
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623832
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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