A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976158



Internal ID22751093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:275144..279283hg38UCSC Ensembl
chrX:191811..195950hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg384140
hg194140
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2227n209
Supporting Variantsnssv17516056, nssv17516055
Samples
Known GenesPLCXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976158
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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