A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958491



Internal ID22733553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118352352..118352352hg38UCSC Ensembl
chrX:117486315..117486315hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443937
Samples
Known GenesWDR44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958491
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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