A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968998



Internal ID22743933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:4824722..4975038hg38UCSC Ensembl
chrY:4692763..4843079hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38150317
hg19150317
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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