A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170792



Internal ID21492118
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 StatusS
Merged Variantsnsv5615934
Supporting Variants
SamplesNA19238
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170792
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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