A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636989



Internal ID7023783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78749733..78757911hg38UCSC Ensembl
Innerchr15:78749733..78757911hg38UCSC Ensembl
Outerchr15:78749233..78758411hg38UCSC Ensembl
chr15:79042075..79050253hg19UCSC Ensembl
Innerchr15:79042075..79050253hg19UCSC Ensembl
Outerchr15:79041575..79050753hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg388179
hg198179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15302003, essv15302002, essv15302004, essv15302001, essv15302005
SamplesHG04144, NA21108, HG03830, NA21090, HG03863
Known GenesLOC646938
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636989
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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