A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257994



Internal ID21399047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149678355..149744968hg38UCSC Ensembl
chrX:148760023..148826629hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3866614
hg1966607
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00731
Known GenesMAGEA11
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257994
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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