A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257604



Internal ID21400012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149742318..149776625hg38UCSC Ensembl
chrX:148823979..148858283hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3834308
hg1934305
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesNA19238
Known GenesHSFX1, HSFX2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257604
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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