A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632723



Internal ID7019534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74382802..74434074hg38UCSC Ensembl
Innerchr13:74382814..74434062hg38UCSC Ensembl
Outerchr13:74382790..74434086hg38UCSC Ensembl
chr13:74956939..75008211hg19UCSC Ensembl
Innerchr13:74956951..75008199hg19UCSC Ensembl
Outerchr13:74956927..75008223hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3851273
hg1951273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14796469
SamplesHG01699
Known GenesLINC00381
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632723
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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