A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276318



Internal ID20485536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3600724..3600724hg38UCSC Ensembl
chr18:3600722..3600722hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764202
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276318
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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