A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616258



Internal ID20989329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82142396..82142756hg38UCSC Ensembl
chr7:81771712..81772072hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160303
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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