A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874823



Internal ID22649777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17660782..17665420hg38UCSC Ensembl
chrX:17678902..17683540hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg384639
hg194639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444621
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874823
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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