A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282584



Internal ID20491802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78072387..78072716hg38UCSC Ensembl
chrX:77327884..77328213hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282584
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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