A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257629



Internal ID21398980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233406..40236154hg38UCSC Ensembl
chr4:40235026..40237774hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382749
hg192749
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730160
Supporting Variants
SamplesHG00731
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257629
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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