A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670441



Internal ID21618746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9332879..9379411hg38UCSC Ensembl
chrY:9170488..9217020hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3846533
hg1946533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170943
SamplesHG02011
Known GenesFAM197Y2, FAM197Y5, TSPY4, TSPY8, TTTY20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670441
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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