A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256131



Internal ID21400443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102338218..102354381hg38UCSC Ensembl
chrX:101593141..101609304hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3816164
hg1916164
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730235
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256131
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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