A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619140



Internal ID20992211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13332608..13337581hg38UCSC Ensembl
chr7:13372233..13377206hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg384974
hg194974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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