A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268395



Internal ID20477613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72211569..72211569hg38UCSC Ensembl
chr8:73123804..73123804hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768080
Supporting Variants
Samples
Known GenesLOC392232
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268395
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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