A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970888



Internal ID22745823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149929491..149949874hg38UCSC Ensembl
chrX:149097709..149118092hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3820384
hg1920384
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515619
Samples
Known GenesCXorf40B, LINC00894
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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