A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561130



Internal ID334117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:153031262..153820289hg38UCSC Ensembl
chr7:152728347..153517374hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38789028
hg19789028
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561130
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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