A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745524



Internal ID20521534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49084433..49084433hg38UCSC Ensembl
chrX:48941344..48941344hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286829
Samples
Known GenesWDR45
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745524
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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