A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591050



Internal ID6631334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63128959..63135181hg38UCSC Ensembl
Innerchr2:63128968..63135172hg38UCSC Ensembl
Outerchr2:63128950..63135190hg38UCSC Ensembl
chr2:63356094..63362316hg19UCSC Ensembl
Innerchr2:63356103..63362307hg19UCSC Ensembl
Outerchr2:63356085..63362325hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg386223
hg196223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10522185
SamplesHG02922
Known GenesWDPCP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591050
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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