A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15291494



Internal ID5293310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72366924..72368726hg38UCSC Ensembl
Innerchr15:72366954..72368696hg38UCSC Ensembl
Outerchr15:72366894..72368756hg38UCSC Ensembl
chr15:72659265..72661067hg19UCSC Ensembl
Innerchr15:72659295..72661037hg19UCSC Ensembl
Outerchr15:72659235..72661097hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636874
Supporting Variants
SamplesHG00593
Known GenesHEXA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15291494
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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