A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732896



Internal ID20508822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23695257..23695257hg38UCSC Ensembl
chrX:23713374..23713374hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732896
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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