A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256437



Internal ID5258253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56250978..56252789hg38UCSC Ensembl
Innerchr15:56251006..56252761hg38UCSC Ensembl
Outerchr15:56250950..56252817hg38UCSC Ensembl
chr15:56543176..56544987hg19UCSC Ensembl
Innerchr15:56543204..56544959hg19UCSC Ensembl
Outerchr15:56543148..56545015hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636580
Supporting Variants
SamplesHG00121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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