A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581742



Internal ID21530246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25601672..25601730hg38UCSC Ensembl
chr7:25641292..25641350hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154671
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581742
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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