A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615934



Internal ID21564239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:626585..626585hg38UCSC Ensembl
chrY:537320..537320hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170792
SamplesNA19238
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615934
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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