A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263694



Internal ID20472912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43935869..43935869hg38UCSC Ensembl
chr2:44163008..44163008hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760309
Supporting Variants
Samples
Known GenesLRPPRC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263694
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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