A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975722



Internal ID22750657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26510779..26515012hg38UCSC Ensembl
chrY:28656926..28661159hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg384234
hg194234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2332n209
Supporting Variantsnssv17517358, nssv17517356, nssv17517357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975722
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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