A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498156



Internal ID20871364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99377332..99418248hg38UCSC Ensembl
chr15:99917537..99958453hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3840917
hg1940917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181815
Samples
Known GenesLRRC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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