A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636437



Internal ID6676544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50101559..50119291hg38UCSC Ensembl
Innerchr15:50101559..50119291hg38UCSC Ensembl
Outerchr15:50101059..50119791hg38UCSC Ensembl
chr15:50393756..50411488hg19UCSC Ensembl
Innerchr15:50393756..50411488hg19UCSC Ensembl
Outerchr15:50393256..50411988hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3817733
hg1917733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15246636
SamplesHG04153
Known GenesATP8B4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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