A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623844



Internal ID6664011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74916093..74919788hg38UCSC Ensembl
Innerchr10:74916098..74919784hg38UCSC Ensembl
Outerchr10:74916089..74919793hg38UCSC Ensembl
chr10:76675851..76679546hg19UCSC Ensembl
Innerchr10:76675856..76679542hg19UCSC Ensembl
Outerchr10:76675847..76679551hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383696
hg193696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863946, essv13863945
SamplesHG01889, HG02339
Known GenesKAT6B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623844
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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