A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557950



Internal ID331028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6797689..6797725hg38UCSC Ensembl
chr6:6797922..6797958hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557950
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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