A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517398



Internal ID22575362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5101394..5112367hg38UCSC Ensembl
chrY:4969435..4980408hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3810974
hg1910974
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972927
Supporting Variants
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517398
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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