A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15316906



Internal ID3421463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88371154..88374245hg38UCSC Ensembl
Innerchr15:88371154..88374245hg38UCSC Ensembl
Outerchr15:88370963..88374415hg38UCSC Ensembl
chr15:88914385..88917476hg19UCSC Ensembl
Innerchr15:88914385..88917476hg19UCSC Ensembl
Outerchr15:88914194..88917646hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383092
hg193092
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637170
Supporting Variants
SamplesHG03060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15316906
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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