A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256236



Internal ID21398928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76145958..76149152hg38UCSC Ensembl
chrX:75365793..75368987hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg383195
hg193195
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730272
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256236
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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