A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969730



Internal ID22744665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92127553..92136323hg38UCSC Ensembl
chrX:91382552..91391322hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg388771
hg198771
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516945
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969730
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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