A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637197



Internal ID6677304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89515971..89518616hg38UCSC Ensembl
Innerchr15:89516471..89518116hg38UCSC Ensembl
Outerchr15:89514971..89519616hg38UCSC Ensembl
chr15:90059202..90061847hg19UCSC Ensembl
Innerchr15:90059702..90061347hg19UCSC Ensembl
Outerchr15:90058202..90062847hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382646
hg192646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317167, essv15317168, essv15317166, essv15317169
SamplesHG00337, HG00178, HG03775, HG02429
Known GenesLINC00928
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637197
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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