A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15327931



Internal ID6074417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96054163..96056697hg38UCSC Ensembl
Innerchr15:96054163..96056697hg38UCSC Ensembl
Outerchr15:96053907..96056919hg38UCSC Ensembl
chr15:96597392..96599926hg19UCSC Ensembl
Innerchr15:96597392..96599926hg19UCSC Ensembl
Outerchr15:96597136..96600148hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637346
Supporting Variants
SamplesNA19462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15327931
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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