A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637049



Internal ID7023843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81978793..81981038hg38UCSC Ensembl
Innerchr15:81978823..81981009hg38UCSC Ensembl
Outerchr15:81978764..81981068hg38UCSC Ensembl
chr15:82271134..82273379hg19UCSC Ensembl
Innerchr15:82271164..82273350hg19UCSC Ensembl
Outerchr15:82271105..82273409hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15307418
SamplesHG02325
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637049
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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