A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464614



Internal ID22522501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20094096..20154531hg38UCSC Ensembl
chrY:22255982..22316417hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3860436
hg1960436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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