A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622736



Internal ID6662905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27871144..27875839hg38UCSC Ensembl
Innerchr10:27871194..27875790hg38UCSC Ensembl
Outerchr10:27871095..27875889hg38UCSC Ensembl
chr10:28160073..28164768hg19UCSC Ensembl
Innerchr10:28160123..28164719hg19UCSC Ensembl
Outerchr10:28160024..28164818hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384696
hg194696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13737698, essv13737695, essv13737702, essv13737696, essv13737701, essv13737699, essv13737700, essv13737694, essv13737697
SamplesHG02725, NA18953, HG01915, NA19068, HG04198, NA19316, NA19000, HG03849, NA18988
Known GenesARMC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622736
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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