A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571747



Internal ID21520129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97183894..97184200hg38UCSC Ensembl
chr7:96813206..96813512hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142825
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571747
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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