A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869807



Internal ID22644742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146428611..146430164hg38UCSC Ensembl
chrX:145510129..145511682hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869807
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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