A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863944



Internal ID3865760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74845345..74847488hg38UCSC Ensembl
Innerchr10:74845394..74847440hg38UCSC Ensembl
Outerchr10:74845297..74847537hg38UCSC Ensembl
chr10:76605103..76607246hg19UCSC Ensembl
Innerchr10:76605152..76607198hg19UCSC Ensembl
Outerchr10:76605055..76607295hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623843
Supporting Variants
SamplesHG03857
Known GenesKAT6B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863944
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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