A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13685252



Internal ID2749506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4867721..4880131hg38UCSC Ensembl
Innerchr10:4867724..4880129hg38UCSC Ensembl
Outerchr10:4867719..4880134hg38UCSC Ensembl
chr10:4909913..4922323hg19UCSC Ensembl
Innerchr10:4909916..4922321hg19UCSC Ensembl
Outerchr10:4909911..4922326hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3812411
hg1912411
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622212
Supporting Variants
SamplesHG02419
Known GenesAKR1C6P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13685252
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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