A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755463



Internal ID20531323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45497640..45497640hg38UCSC Ensembl
chr1:45963312..45963312hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259446
Samples
Known GenesCCDC163P
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755463
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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