A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502395



Internal ID20875640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77197380..77214796hg38UCSC Ensembl
chr16:77231277..77248693hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3817417
hg1917417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031994
Samples
Known GenesMON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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