A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606212



Internal ID21554517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112117363..112117363hg38UCSC Ensembl
chrX:111360591..111360591hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164912
SamplesHG02818
Known GenesZCCHC16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606212
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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