A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969053



Internal ID22743988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14541737..14551300hg38UCSC Ensembl
chrY:16653617..16663180hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg389564
hg199564
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517074
Samples
Known GenesNLGN4Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969053
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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