A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419294



Internal ID21076847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155615017..155617187hg38UCSC Ensembl
chr7:155407711..155409881hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382171
hg192171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7195n223
Supporting Variantsnssv18151407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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