A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13860900



Internal ID3862716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71649902..71651062hg38UCSC Ensembl
Innerchr10:71649932..71651032hg38UCSC Ensembl
Outerchr10:71649872..71651092hg38UCSC Ensembl
chr10:73409659..73410819hg19UCSC Ensembl
Innerchr10:73409689..73410789hg19UCSC Ensembl
Outerchr10:73409629..73410849hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623780
Supporting Variants
SamplesHG04227
Known GenesCDH23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13860900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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