A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636656



Internal ID7023450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60119614..60120225hg38UCSC Ensembl
Innerchr15:60119664..60120175hg38UCSC Ensembl
Outerchr15:60119548..60120291hg38UCSC Ensembl
chr15:60411813..60412424hg19UCSC Ensembl
Innerchr15:60411863..60412374hg19UCSC Ensembl
Outerchr15:60411747..60412490hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261142
SamplesNA19657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636656
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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