A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256653



Internal ID21399703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149678415..149732014hg38UCSC Ensembl
chrX:148760083..148813674hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3853600
hg1953592
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00733
Known GenesMAGEA11
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256653
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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