A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637169



Internal ID7023963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88350512..88353552hg38UCSC Ensembl
Innerchr15:88350524..88353540hg38UCSC Ensembl
Outerchr15:88350500..88353564hg38UCSC Ensembl
chr15:88893743..88896783hg19UCSC Ensembl
Innerchr15:88893755..88896771hg19UCSC Ensembl
Outerchr15:88893731..88896795hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383041
hg193041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15316905, essv15316904
SamplesNA19026, NA19025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637169
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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