A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571396



Internal ID21519774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82099411..82099747hg38UCSC Ensembl
chr7:81728727..81729063hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158826
SamplesHG00732
Known GenesCACNA2D1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571396
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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