A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256189



Internal ID21399858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51693341..51700302hg38UCSC Ensembl
chrX:51436063..51443023hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg386962
hg196961
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730130
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256189
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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