A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708558



Internal ID21198452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76141880..76153240hg38UCSC Ensembl
chrX:75361715..75373075hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3811361
hg1911361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820782
Supporting Variants
SamplesCHM13
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708558
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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