A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258421



Internal ID21400043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233251..40235440hg38UCSC Ensembl
chr4:40234871..40237060hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382190
hg192190
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730160
Supporting Variants
SamplesNA19238
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258421
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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