A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764236



Internal ID3766052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43164970..43165801hg38UCSC Ensembl
Innerchr10:43165020..43165751hg38UCSC Ensembl
Outerchr10:43164920..43165851hg38UCSC Ensembl
chr10:43660418..43661249hg19UCSC Ensembl
Innerchr10:43660468..43661199hg19UCSC Ensembl
Outerchr10:43660368..43661299hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623038
Supporting Variants
SamplesNA19144
Known GenesCSGALNACT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764236
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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