A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970024



Internal ID22744959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2916649..2919849hg38UCSC Ensembl
chrY:2784690..2787890hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970024
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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