A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260461



Internal ID20469679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77586985..77586985hg38UCSC Ensembl
chr5:76882810..76882810hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260461
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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