A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738405



Internal ID162071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11967400..11969225hg38UCSC Ensembl
chrY:14088106..14089931hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738405
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002484


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