A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052977



Internal ID21962211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112874260..112874260hg38UCSC Ensembl
chrX:112117488..112117488hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052977
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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