A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257242



Internal ID21399881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52070847..52192188hg38UCSC Ensembl
chrX:51813943..51935284hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38121342
hg19121342
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730085
Supporting Variants
SamplesNA19238
Known GenesMAGED4, MAGED4B, SNORA11D, SNORA11E
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257242
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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