A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732474



Internal ID20508398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26554049..26554462hg38UCSC Ensembl
chr18:24134013..24134426hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267063
Samples
Known GenesKCTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732474
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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