A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141363



Internal ID20708403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2955863..2956553hg38UCSC Ensembl
chr6:2956097..2956787hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406290
Supporting Variants
Samples
Known GenesSERPINB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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