A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271951



Internal ID20481169
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 StatusS
Merged Variantsnsv4732368
Supporting Variants
Samples
Known GenesPAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271951
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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