A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928175



Internal ID21348244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82099411..82099748hg38UCSC Ensembl
chr7:81728727..81729064hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198614
SamplesHG002
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928175
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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