A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575072



Internal ID21523497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151031225..151031300hg38UCSC Ensembl
chr3:150749012..150749087hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138191
SamplesHG02587
Known GenesCLRN1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575072
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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