A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257732



Internal ID21398395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149668972..149732019hg38UCSC Ensembl
chrX:148750640..148813679hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3863048
hg1963040
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00513
Known GenesMAGEA11
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257732
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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