A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882412



Internal ID22657389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7387589..7907416hg38UCSC Ensembl
chrY:7255630..7775457hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38519828
hg19519828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457370
Samples
Known GenesTTTY12, TTTY16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882412
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer