A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965848



Internal ID22740783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61202586..61202586hg38UCSC Ensembl
chr8:62115145..62115145hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965848
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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