A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224479



Internal ID20791519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96922301..96927500hg38UCSC Ensembl
chr6:97370177..97375376hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600605
Supporting Variants
Samples
Known GenesKLHL32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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