A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146061



Internal ID20713101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85627264..85633180hg38UCSC Ensembl
chr6:86336982..86342898hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg385917
hg195917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409175
Supporting Variants
Samples
Known GenesSYNCRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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