A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882063



Internal ID22657040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7813971..7814030hg38UCSC Ensembl
chrY:7682012..7682071hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882063
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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