A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15137575



Internal ID6885413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19800619..19807270hg38UCSC Ensembl
Innerchr15:19800769..19807120hg38UCSC Ensembl
Outerchr15:19800469..19807420hg38UCSC Ensembl
chr15:20005872..20012523hg19UCSC Ensembl
Innerchr15:20006022..20012373hg19UCSC Ensembl
Outerchr15:20005722..20012673hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg386652
hg196652
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635717
Supporting Variants
SamplesNA21103
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15137575
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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