A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13665703



Internal ID3667519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1572350..1573239hg38UCSC Ensembl
Innerchr10:1572385..1573205hg38UCSC Ensembl
Outerchr10:1572316..1573274hg38UCSC Ensembl
chr10:1614545..1615434hg19UCSC Ensembl
Innerchr10:1614580..1615400hg19UCSC Ensembl
Outerchr10:1614511..1615469hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622107
Supporting Variants
SamplesHG01851
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13665703
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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