A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278829



Internal ID20488047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68903897..68903989hg38UCSC Ensembl
chrX:68123740..68123832hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278829
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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