A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170601



Internal ID21501135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2578898..2578898hg38UCSC Ensembl
chrY:2446939..2446939hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614896
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170601
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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