A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589867



Internal ID6977197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14024338..14043513hg38UCSC Ensembl
Innerchr2:14024338..14043513hg38UCSC Ensembl
Outerchr2:14023838..14044013hg38UCSC Ensembl
chr2:14164463..14183638hg19UCSC Ensembl
Innerchr2:14164463..14183638hg19UCSC Ensembl
Outerchr2:14163963..14184138hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3819176
hg1919176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10414260, essv10414259
SamplesHG02332, HG01357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589867
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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