A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508631



Internal ID20881935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62290605..62321380hg38UCSC Ensembl
chr15:62582804..62613579hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3830776
hg1930776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025582
Samples
Known GenesMIR8067
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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