A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970095



Internal ID22745030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140014046..140021280hg38UCSC Ensembl
chrX:139096205..139103439hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg387235
hg197235
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970095
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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