A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963719



Internal ID22738654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41195541..41195541hg38UCSC Ensembl
chr8:41053060..41053060hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963719
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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