A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734963



Internal ID20510903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106960383..106960594hg38UCSC Ensembl
chr1:107503005..107503216hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734963
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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