A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756337



Internal ID20532197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76975160..76975160hg38UCSC Ensembl
chr18:74687116..74687116hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756337
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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