A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735712



Internal ID20511655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123959736..123959828hg38UCSC Ensembl
chr3:123678583..123678675hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273016
Samples
Known GenesCCDC14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735712
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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