A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256444



Internal ID5009689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56374996..56413063hg38UCSC Ensembl
Innerchr15:56374996..56413063hg38UCSC Ensembl
Outerchr15:56374496..56413563hg38UCSC Ensembl
chr15:56667194..56705261hg19UCSC Ensembl
Innerchr15:56667194..56705261hg19UCSC Ensembl
Outerchr15:56666694..56705761hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3838068
hg1938068
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636583
Supporting Variants
SamplesNA18507
Known GenesTEX9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256444
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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