A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972259



Internal ID22747194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141585252..141616288hg38UCSC Ensembl
chrX:140673374..140704416hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3831037
hg1931043
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515558, nssv17515557
Samples
Known GenesSPANXA1, SPANXA2, SPANXA2-OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972259
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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