A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263187



Internal ID20472405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43181881..43181881hg38UCSC Ensembl
chr10:43677329..43677329hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757198
Supporting Variants
Samples
Known GenesCSGALNACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263187
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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