A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107759



Internal ID22016992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152182526..152182855hg38UCSC Ensembl
chrX:151350998..151351327hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639177
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107759
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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