A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636674



Internal ID7023468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60869658..60871309hg38UCSC Ensembl
Innerchr15:60869680..60871288hg38UCSC Ensembl
Outerchr15:60869637..60871331hg38UCSC Ensembl
chr15:61161857..61163508hg19UCSC Ensembl
Innerchr15:61161879..61163487hg19UCSC Ensembl
Outerchr15:61161836..61163530hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15263041
SamplesNA18957
Known GenesRORA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636674
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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