A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517424



Internal ID22575388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9314071..9319736hg38UCSC Ensembl
chrY:9151680..9157345hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg385666
hg195666
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971669
Supporting Variants
Samples
Known GenesRBMY1A3P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517424
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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