A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732368



Internal ID20508292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196827828..196827973hg38UCSC Ensembl
chr3:196554699..196554844hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271951
Samples
Known GenesPAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732368
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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