A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576514



Internal ID21524954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98232895..98240422hg38UCSC Ensembl
chr1:98698451..98705978hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg387528
hg197528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067185
SamplesHG02011
Known GenesLOC729987
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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