A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437109



Internal ID22494979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35765577..35783679hg38UCSC Ensembl
chr6:35733354..35751456hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3818103
hg1918103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899780
Supporting Variants
Samples
Known GenesCLPSL1, CLPSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437109
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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