A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886386



Internal ID22661373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7336526..7336695hg38UCSC Ensembl
chrY:7204567..7204736hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460039
Samples
Known GenesPRKY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886386
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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