A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962220



Internal ID22737009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43181881..43181881hg38UCSC Ensembl
chr10:43677329..43677329hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363511
Samples
Known GenesCSGALNACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962220
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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