A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975552



Internal ID22750487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12131273..12132372hg38UCSC Ensembl
chrY:14251979..14253078hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517048
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975552
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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