A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13974942



Internal ID3974760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130262980..130328381hg38UCSC Ensembl
Innerchr10:130262980..130328381hg38UCSC Ensembl
Outerchr10:130262480..130328881hg38UCSC Ensembl
chr10:132061244..132126645hg19UCSC Ensembl
Innerchr10:132061244..132126645hg19UCSC Ensembl
Outerchr10:132060744..132127145hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3865402
hg1965402
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624930
Supporting Variants
SamplesHG03629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13974942
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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