A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975464



Internal ID22750399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12378990..12554562hg38UCSC Ensembl
chrY:14491215..14666496hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38175573
hg19175282
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517054
Samples
Known GenesGYG2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975464
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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