A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976981



Internal ID22751916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12390193..12408233hg38UCSC Ensembl
chrY:14501988..14520032hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3818041
hg1918045
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517055
Samples
Known GenesGYG2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976981
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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