A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624930



Internal ID7011780
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13974942
SamplesHG03629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624930
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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