A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160277



Internal ID20727317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82010864..82011414hg38UCSC Ensembl
chr7:81640180..81640730hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606989
Supporting Variants
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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