A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256693



Internal ID21400623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102338174..102348796hg38UCSC Ensembl
chrX:101593097..101603719hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3810623
hg1910623
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730235
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256693
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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