A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257251



Internal ID21398485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149599118..149657330hg38UCSC Ensembl
chrX:148680780..148738998hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3858213
hg1958219
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00514
Known GenesTMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257251
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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