A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257658



Internal ID21399769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51692832..51700382hg38UCSC Ensembl
chrX:51436002..51443400hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg387551
hg197399
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730130
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257658
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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