A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899780



Internal ID22674914
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 StatusM
Merged Variants
Supporting Variantsnssv17437109
Samples
Known GenesCLPSL1, CLPSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899780
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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