A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050637



Internal ID21959870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120016947..120016947hg38UCSC Ensembl
chrX:119150904..119150904hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050637
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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