A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977269



Internal ID22752204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5357348..5373374hg38UCSC Ensembl
chrY:5225389..5241415hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3816027
hg1916027
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517400
Samples
Known GenesPCDH11Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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