A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267107



Internal ID20476325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48965772..48965772hg38UCSC Ensembl
chrX:48822179..48822179hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741578
Supporting Variants
Samples
Known GenesKCND1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267107
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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