A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421483



Internal ID21079036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146835068..146934872hg38UCSC Ensembl
chr7:146532160..146631964hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3899805
hg1999805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7164n223
Supporting Variantsnssv18155903
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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