A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743607



Internal ID20519596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65450506..65450506hg38UCSC Ensembl
chrX:64670386..64670386hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743607
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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