A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615523



Internal ID21563828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:628682..628682hg38UCSC Ensembl
chrY:539417..539417hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171010
SamplesNA19239
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615523
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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