A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579134



Internal ID21527610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34883655..34884588hg38UCSC Ensembl
chr1:35349256..35350189hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065133
SamplesNA19983
Known GenesDLGAP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579134
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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