A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506934



Internal ID20880222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63423748..63425101hg38UCSC Ensembl
chr15:63715947..63717300hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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