A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977488



Internal ID22752423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19046270..19069490hg38UCSC Ensembl
chrY:21208156..21231376hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3823221
hg1923221
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517097
Samples
Known GenesTTTY14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977488
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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