A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558604



Internal ID331663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97280124..97284930hg38UCSC Ensembl
chr7:96909436..96914242hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384807
hg194807
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558604
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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