A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762972



Internal ID20538832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58863519..58863519hg38UCSC Ensembl
chr18:56530751..56530751hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291362
Samples
Known GenesZNF532
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762972
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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