A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710461



Internal ID21198449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153066026..153084040hg38UCSC Ensembl
chrX:152234392..152349893hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3818015
hg19115502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820271
Supporting Variants
SamplesCHM13
Known GenesPNMA6A, PNMA6C
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710461
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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