A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571851



Internal ID21763894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82264825..82291197hg38UCSC Ensembl
chr7:81894141..81920513hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3826373
hg1926373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001221
Supporting Variants
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571851
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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