A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968768



Internal ID22743703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145240431..145253820hg38UCSC Ensembl
chrX:144321951..144335340hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3813390
hg1913390
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515583
Samples
Known GenesSPANXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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