A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972736



Internal ID22747671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98396082..98398032hg38UCSC Ensembl
chrX:97651080..97653030hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg381951
hg191951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2290n209
Supporting Variantsnssv17517001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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