A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561074



Internal ID334061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97437046..97460379hg38UCSC Ensembl
chr7:97066358..97089691hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3823334
hg1923334
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561074
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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