A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978449



Internal ID22753384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5101759..5107532hg38UCSC Ensembl
chrY:4969800..4975573hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg385774
hg195774
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517399
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978449
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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