A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256421



Internal ID21398431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154354649..154416288hg38UCSC Ensembl
chrX:153583017..153644627hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3861640
hg1961611
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730161
Supporting Variants
SamplesHG00513
Known GenesDNASE1L1, EMD, FLNA, RPL10, SNORA70, TAZ
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256421
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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