A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462346



Internal ID22520231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13606090..13619502hg38UCSC Ensembl
chrY:15717970..15731382hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3813413
hg1913413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462346
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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