A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979308



Internal ID22754243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63463917..63474793hg38UCSC Ensembl
chrX:62683797..62694673hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3810877
hg1910877
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516529, nssv17516528
Samples
Known GenesLOC92249
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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