A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589796



Internal ID6977126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10293243..10298739hg38UCSC Ensembl
Innerchr2:10293293..10298689hg38UCSC Ensembl
Outerchr2:10293193..10298789hg38UCSC Ensembl
chr2:10433369..10438865hg19UCSC Ensembl
Innerchr2:10433419..10438815hg19UCSC Ensembl
Outerchr2:10433319..10438915hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385497
hg195497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10406916, essv10406915, essv10406917, essv10406914
SamplesHG00114, HG00121, HG00116, NA12776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589796
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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