A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554731



Internal ID327908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98041241..98041280hg38UCSC Ensembl
chr7:97670553..97670592hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3840
hg1940
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554731
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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