A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756232



Internal ID20532092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56689833..56689833hg38UCSC Ensembl
chr18:54357064..54357064hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258920
Samples
Known GenesWDR7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756232
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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