A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13665798



Internal ID3667614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1723223..1726384hg38UCSC Ensembl
Innerchr10:1723273..1726334hg38UCSC Ensembl
Outerchr10:1723121..1726486hg38UCSC Ensembl
chr10:1765417..1768578hg19UCSC Ensembl
Innerchr10:1765467..1768528hg19UCSC Ensembl
Outerchr10:1765315..1768680hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383162
hg193162
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622110
Supporting Variants
SamplesHG00368
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13665798
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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