A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733773



Internal ID20509703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161281745..161281822hg38UCSC Ensembl
chr1:161251535..161251612hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267748
Samples
Known GenesPCP4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733773
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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