A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744876



Internal ID20520880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47848687..47848687hg38UCSC Ensembl
chrX:47708086..47708086hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288702
Samples
Known GenesZNF81
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744876
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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