A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057277



Internal ID21966510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:156009241..156009241hg38UCSC Ensembl
chrX:155238906..155238906hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645442
Samples
Known GenesIL9R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057277
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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