A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975034



Internal ID22749969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3313440..3325474hg38UCSC Ensembl
chrY:3181481..3193515hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3812035
hg1912035
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975034
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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