A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258383



Internal ID21399394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149678356..149734328hg38UCSC Ensembl
chrX:148760024..148815988hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3855973
hg1955965
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00732
Known GenesMAGEA11
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258383
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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