A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170796



Internal ID21488951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:628979..628979hg38UCSC Ensembl
chrY:539714..539714hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621519
Supporting Variants
SamplesNA18939
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170796
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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