A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258684



Internal ID21398512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52040135..52176862hg38UCSC Ensembl
chrX:51783231..51919958hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38136728
hg19136728
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730085
Supporting Variants
SamplesHG00514
Known GenesMAGED4, MAGED4B, SNORA11D, SNORA11E
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258684
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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