A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664673



Internal ID3666489
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622096
Supporting Variants
SamplesHG03547
Known GenesWDR37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664673
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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