A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138969



Internal ID20706009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124628545..124629299hg38UCSC Ensembl
chr6:124949691..124950445hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602066
Supporting Variants
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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