A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589918



Internal ID6977248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15677153..15683962hg38UCSC Ensembl
Innerchr2:15677153..15683962hg38UCSC Ensembl
Outerchr2:15676967..15684139hg38UCSC Ensembl
chr2:15817277..15824086hg19UCSC Ensembl
Innerchr2:15817277..15824086hg19UCSC Ensembl
Outerchr2:15817091..15824263hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg386810
hg196810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10417867
SamplesHG04144
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589918
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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