A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971277



Internal ID22746212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7089658..7091657hg38UCSC Ensembl
chrY:6957699..6959698hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517411
Samples
Known GenesTBL1Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971277
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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