A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559198



Internal ID332239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97420352..97420403hg38UCSC Ensembl
chr7:97049664..97049715hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385932
hg195932
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559198
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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