A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496844



Internal ID20870047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87921021..87937997hg38UCSC Ensembl
chr16:87954627..87971603hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3816977
hg1916977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033138
Samples
Known GenesCA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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