A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15276534



Internal ID5278350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67575945..67577058hg38UCSC Ensembl
Innerchr15:67575945..67577058hg38UCSC Ensembl
Outerchr15:67575628..67577452hg38UCSC Ensembl
chr15:67868283..67869396hg19UCSC Ensembl
Innerchr15:67868283..67869396hg19UCSC Ensembl
Outerchr15:67867966..67869790hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636790
Supporting Variants
SamplesHG04186
Known GenesMAP2K5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15276534
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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