A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257181



Internal ID21399464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233334..40235450hg38UCSC Ensembl
chr4:40234954..40237070hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382117
hg192117
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730160
Supporting Variants
SamplesHG00733
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257181
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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