A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622096



Internal ID6662266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1064715..1071589hg38UCSC Ensembl
chr10:1110655..1117529hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg386875
hg196875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13664672, essv13664673, essv13664671
SamplesHG03547, HG02614, HG02813
Known GenesWDR37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622096
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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