A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878482



Internal ID22653447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140411719..140420804hg38UCSC Ensembl
chrX:139493884..139502969hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg389086
hg199086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2300n209
Supporting Variantsnssv17440540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878482
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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