A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555813



Internal ID328963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109654790..109791530hg38UCSC Ensembl
chr7:109294847..109431587hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38136741
hg19136741
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555813
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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