A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138880



Internal ID20705920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123945986..124033511hg38UCSC Ensembl
chr6:124267131..124354656hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3887526
hg1987526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608418
Supporting Variants
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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