A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506078



Internal ID20879353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87833995..87886965hg38UCSC Ensembl
chr16:87867601..87920571hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3852971
hg1952971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033123
Samples
Known GenesMIR6775, SLC7A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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