A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257856



Internal ID21399079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135147447..135247901hg38UCSC Ensembl
chrX:134281374..134381848hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38100455
hg19100475
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730233
Supporting Variants
SamplesHG00731
Known GenesCXorf48
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257856
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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