A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452107



Internal ID22509979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11907821..11907821hg38UCSC Ensembl
chrY:14028527..14028527hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452107
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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