A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257803



Internal ID21399594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218792..6220343hg38UCSC Ensembl
chrX:6136833..6138384hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730244
Supporting Variants
SamplesHG00733
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257803
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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