A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969706



Internal ID22744641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23837765..23854556hg38UCSC Ensembl
chrX:23855882..23872673hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3816792
hg1916792
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516005
Samples
Known GenesAPOO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969706
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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