A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13983512



Internal ID6645150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132820048..132833523hg38UCSC Ensembl
chr10:134633552..134647027hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3813476
hg1913476
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625008
Supporting Variants
SamplesNA20800
Known GenesTTC40
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13983512
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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