A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738426



Internal ID162092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13308354..13312158hg38UCSC Ensembl
chrY:15420234..15424038hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg383805
hg193805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416542
Supporting Variants
Samples
Known GenesUTY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738426
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000567


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