A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741578



Internal ID20517555
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 StatusM
Merged Variants
Supporting Variantsnssv16267107
Samples
Known GenesKCND1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741578
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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