A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950996



Internal ID22726385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139002765..139002765hg38UCSC Ensembl
chr6:139323902..139323902hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950996
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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