A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15284111



Internal ID5140534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70735243..70761071hg38UCSC Ensembl
Innerchr15:70735743..70760571hg38UCSC Ensembl
Outerchr15:70734243..70762071hg38UCSC Ensembl
chr15:71027582..71053410hg19UCSC Ensembl
Innerchr15:71028082..71052910hg19UCSC Ensembl
Outerchr15:71026582..71054410hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825829
hg1925829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636844
Supporting Variants
SamplesNA18572
Known GenesUACA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15284111
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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