A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15248698



Internal ID2585630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51600887..51607532hg38UCSC Ensembl
Innerchr15:51601387..51607032hg38UCSC Ensembl
Outerchr15:51599887..51608532hg38UCSC Ensembl
chr15:51893084..51899729hg19UCSC Ensembl
Innerchr15:51893584..51899229hg19UCSC Ensembl
Outerchr15:51892084..51900729hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg386646
hg196646
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636472
Supporting Variants
SamplesHG02286
Known GenesDMXL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15248698
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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