A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142012



Internal ID20709052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158903809..158910525hg38UCSC Ensembl
chr6:159324841..159331557hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg386717
hg196717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614335
Supporting Variants
Samples
Known GenesC6orf99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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