A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968992



Internal ID22743927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15721247..15736987hg38UCSC Ensembl
chrY:17833127..17848867hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3815741
hg1915741
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968992
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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