A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975414



Internal ID22750349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142547137..142554888hg38UCSC Ensembl
chrX:141634923..141642674hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg387752
hg197752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975414
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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