A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317261



Internal ID5319077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90247166..90250794hg38UCSC Ensembl
Innerchr15:90247230..90250731hg38UCSC Ensembl
Outerchr15:90247103..90250858hg38UCSC Ensembl
chr15:90790398..90794026hg19UCSC Ensembl
Innerchr15:90790462..90793963hg19UCSC Ensembl
Outerchr15:90790335..90794090hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383629
hg193629
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637217
Supporting Variants
SamplesHG04198
Known GenesCIB1, TTLL13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317261
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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