A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968074



Internal ID22743009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7632187..7659285hg38UCSC Ensembl
chrY:7500228..7527326hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3827099
hg1927099
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968074
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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