A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975986



Internal ID22750921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141690049..141697474hg38UCSC Ensembl
chrX:140778210..140785631hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg387426
hg197422
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515563, nssv17515564
Samples
Known GenesSPANXD, SPANXE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975986
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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