A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669032



Internal ID21617337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1271213..1271395hg38UCSC Ensembl
chrY:1340106..1340288hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169217
SamplesHG03125
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669032
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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