A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884006



Internal ID22658988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148253498..148255408hg38UCSC Ensembl
chrX:147335018..147336928hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381911
hg191911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884006
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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