A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574042



Internal ID21522453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11037589..11046271hg38UCSC Ensembl
chr1:11097646..11106328hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg388683
hg198683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059913
SamplesHG02011
Known GenesMASP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574042
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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