A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430799



Internal ID21088352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146013713..146019926hg38UCSC Ensembl
chr7:145710806..145717019hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg386214
hg196214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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