A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968444



Internal ID22743379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:276309..280083hg38UCSC Ensembl
chrX:192976..196750hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg383775
hg193775
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2227n209
Supporting Variantsnssv17516062, nssv17516063
Samples
Known GenesPLCXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968444
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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