A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10415061



Internal ID2223130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15016426..15121840hg38UCSC Ensembl
Innerchr2:15016458..15121808hg38UCSC Ensembl
Outerchr2:15016394..15121872hg38UCSC Ensembl
chr2:15156550..15261964hg19UCSC Ensembl
Innerchr2:15156582..15261932hg19UCSC Ensembl
Outerchr2:15156518..15261996hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38105415
hg19105415
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3589904
Supporting Variants
SamplesHG01997
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10415061
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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