A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13941305



Internal ID4421413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114684410..114690139hg38UCSC Ensembl
Innerchr10:114684425..114690124hg38UCSC Ensembl
Outerchr10:114684395..114690154hg38UCSC Ensembl
chr10:116444169..116449898hg19UCSC Ensembl
Innerchr10:116444184..116449883hg19UCSC Ensembl
Outerchr10:116444154..116449913hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385730
hg195730
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624617
Supporting Variants
SamplesHG03937
Known GenesABLIM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13941305
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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