A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15259199



Internal ID1483771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57294888..57295691hg38UCSC Ensembl
Innerchr15:57294897..57295682hg38UCSC Ensembl
Outerchr15:57294879..57295700hg38UCSC Ensembl
chr15:57587086..57587889hg19UCSC Ensembl
Innerchr15:57587095..57587880hg19UCSC Ensembl
Outerchr15:57587077..57587898hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636607
Supporting Variants
SamplesHG01365
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15259199
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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