A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15321631



Internal ID4275862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92849762..92863848hg38UCSC Ensembl
Innerchr15:92849792..92863818hg38UCSC Ensembl
Outerchr15:92849732..92863878hg38UCSC Ensembl
chr15:93392992..93407078hg19UCSC Ensembl
Innerchr15:93393022..93407048hg19UCSC Ensembl
Outerchr15:93392962..93407108hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3814087
hg1914087
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637271
Supporting Variants
SamplesHG03838
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15321631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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