A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146056



Internal ID20713096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85605601..85612800hg38UCSC Ensembl
chr6:86315319..86322518hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397805
Supporting Variants
Samples
Known GenesSYNCRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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