A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053864



Internal ID21963097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77790967..77790967hg38UCSC Ensembl
chrX:77046431..77046431hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053864
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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