A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15255915



Internal ID2591534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55363348..55364858hg38UCSC Ensembl
Innerchr15:55363348..55364858hg38UCSC Ensembl
Outerchr15:55362930..55365269hg38UCSC Ensembl
chr15:55655546..55657056hg19UCSC Ensembl
Innerchr15:55655546..55657056hg19UCSC Ensembl
Outerchr15:55655128..55657467hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636558
Supporting Variants
SamplesHG02298
Known GenesCCPG1, DYX1C1-CCPG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15255915
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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