A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258443



Internal ID21400036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187418975..187426287hg38UCSC Ensembl
chr3:187136763..187144075hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg387313
hg197313
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730103
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258443
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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