A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224572



Internal ID20791612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88444601..88448600hg38UCSC Ensembl
chr6:89154320..89158319hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412457
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00293


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