A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970852



Internal ID22745787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11965762..11969446hg38UCSC Ensembl
chrY:14086468..14090152hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg383685
hg193685
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970852
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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