A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868226



Internal ID22643161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153481271..153481322hg38UCSC Ensembl
chrX:152746729..152746780hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432227
Samples
Known GenesHAUS7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868226
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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