A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256452



Internal ID21399863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149654076..149749222hg38UCSC Ensembl
chrX:148735744..148830883hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3895147
hg1995140
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesNA19238
Known GenesMAGEA11
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256452
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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