A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637097



Internal ID6677204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84645188..84682110hg38UCSC Ensembl
chr15:85188419..85225341hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3836923
hg1936923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15313630
SamplesHG02885
Known GenesNMB, SEC11A, WDR73
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637097
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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