A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637262



Internal ID6677369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92402352..92407464hg38UCSC Ensembl
Innerchr15:92402378..92407438hg38UCSC Ensembl
Outerchr15:92402326..92407490hg38UCSC Ensembl
chr15:92945582..92950694hg19UCSC Ensembl
Innerchr15:92945608..92950668hg19UCSC Ensembl
Outerchr15:92945556..92950720hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385113
hg195113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15320965
SamplesHG03968
Known GenesST8SIA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637262
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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