A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416081



Internal ID21073634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143239704..143248923hg38UCSC Ensembl
chr7:142936797..142946016hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg389220
hg199220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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