A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637218



Internal ID6677325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90252532..90266165hg38UCSC Ensembl
chr15:90795764..90809397hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3813634
hg1913634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317262
SamplesHG03781
Known GenesCIB1, NGRN, TTLL13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637218
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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