A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462838



Internal ID22520723
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 StatusS
Merged Variantsnsv5979256
Supporting Variants
Samples
Known GenesNLGN4Y
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462838
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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