A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969372



Internal ID22744307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13479445..13480966hg38UCSC Ensembl
chrY:15591325..15592846hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381522
hg191522
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517060
Samples
Known GenesUTY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969372
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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