A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647351



Internal ID21839398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119897100..119897448hg38UCSC Ensembl
chrX:119031063..119031411hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106425
Supporting Variants
Samples
Known GenesAKAP14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647351
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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