A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666668



Internal ID21614974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:629043..629192hg38UCSC Ensembl
chrY:539778..539927hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171012
SamplesHG00731
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666668
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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