A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422789



Internal ID22480659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139070269..139070269hg38UCSC Ensembl
chr6:139391406..139391406hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422789
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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