A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870926



Internal ID22645863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23997299..23997647hg38UCSC Ensembl
chrX:24015416..24015764hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466849
Samples
Known GenesKLHL15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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