A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495694



Internal ID20868888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77658432..77812272hg38UCSC Ensembl
chr16:77692329..77846169hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38153841
hg19153841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032030
Samples
Known GenesNUDT7, VAT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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