A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557918



Internal ID330997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37371895..37372756hg38UCSC Ensembl
chr9:37371892..37372753hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557918
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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