A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423936



Internal ID21081489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143165801..143196800hg38UCSC Ensembl
chr7:142862894..142893893hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3831000
hg1931000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7156n223
Supporting Variantsnssv18152464
Samples
Known GenesTAS2R39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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