A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499377



Internal ID20872596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77987298..78048236hg38UCSC Ensembl
chr16:78021195..78082133hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3860939
hg1960939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2943n223
Supporting Variantsnssv18032058
Samples
Known GenesCLEC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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