A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581693



Internal ID21530196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70840012..70840116hg38UCSC Ensembl
chr4:71705729..71705833hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133196
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581693
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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