A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609776



Internal ID21558081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1280976..1280976hg38UCSC Ensembl
chrY:1349869..1349869hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169221, nssv17169222
SamplesHG00512, NA19238
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609776
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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