A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141319



Internal ID20708359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28991376..29188824hg38UCSC Ensembl
chr6:28959153..29156601hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38197449
hg19197449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413018
Supporting Variants
Samples
Known GenesLOC100129636, OR2B3, OR2J2, OR2J3, OR2W1, ZNF311
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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