A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6977n223



Internal ID22809945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82171131..82890285hg38UCSC Ensembl
chr7:81800447..82519601hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38719155
hg19719155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6609199, nsv6611662, nsv6617998
Samples
Known GenesCACNA2D1, PCLO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6977n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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