A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755771



Internal ID20531631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95631254..95631254hg38UCSC Ensembl
chr5:94966958..94966958hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755771
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer