A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142601



Internal ID20709641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163169638..163174733hg38UCSC Ensembl
chr6:163590670..163595765hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg385096
hg195096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614935
Supporting Variants
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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