A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267758



Internal ID20476976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75379901..75379964hg38UCSC Ensembl
chrX:74599736..74599799hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762004
Supporting Variants
Samples
Known GenesZDHHC15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267758
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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