A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256178



Internal ID21399830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233251..40235411hg38UCSC Ensembl
chr4:40234871..40237031hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382161
hg192161
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)nssv16256178
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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