A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956995



Internal ID22732145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61310572..61310572hg38UCSC Ensembl
chr5:60606399..60606399hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956995
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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