A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589766



Internal ID6977096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9111525..9122088hg38UCSC Ensembl
Innerchr2:9111560..9122054hg38UCSC Ensembl
Outerchr2:9111491..9122123hg38UCSC Ensembl
chr2:9251654..9262217hg19UCSC Ensembl
Innerchr2:9251689..9262183hg19UCSC Ensembl
Outerchr2:9251620..9262252hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3810564
hg1910564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10404288
SamplesHG03770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589766
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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