A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619081



Internal ID20992152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:788176..823153hg38UCSC Ensembl
chr7:827813..862790hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3834978
hg1934978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158953
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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