A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13855017



Internal ID2983459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69297614..69300767hg38UCSC Ensembl
Innerchr10:69297620..69300762hg38UCSC Ensembl
Outerchr10:69297609..69300773hg38UCSC Ensembl
chr10:71057370..71060523hg19UCSC Ensembl
Innerchr10:71057376..71060518hg19UCSC Ensembl
Outerchr10:71057365..71060529hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623741
Supporting Variants
SamplesHG02634
Known GenesHK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13855017
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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