A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512194



Internal ID20885525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89897470..89902304hg38UCSC Ensembl
chr15:90440702..90445536hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384835
hg194835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026909
Samples
Known GenesC15orf38, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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