A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820782



Internal ID21266120
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 StatusM
Merged Variants
Supporting Variantsnssv13710597, nssv13708558
SamplesCHM13, CHM1
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820782
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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