A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979256



Internal ID22754191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14186304..14549573hg38UCSC Ensembl
chrY:16298184..16661453hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38363270
hg19363270
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462838
Samples
Known GenesNLGN4Y
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979256
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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