A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004222



Internal ID70450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113134263..113136326hg38UCSC Ensembl
chr7:112774318..112776381hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg382064
hg192064
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004222
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.031221


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