A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110791



Internal ID22020024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56689828..56689828hg38UCSC Ensembl
chr18:54357059..54357059hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635909
Samples
Known GenesWDR7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110791
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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