A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637216



Internal ID6677323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90242762..90247368hg38UCSC Ensembl
chr15:90785994..90790600hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384607
hg194607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317258, essv15317259, essv15317260, essv15317257
SamplesNA18616, NA19771, HG01384, NA19093
Known GenesCIB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637216
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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