A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606110



Internal ID20979181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1759924..1783829hg38UCSC Ensembl
chr7:1799560..1823465hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3823906
hg1923906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6538n223
Supporting Variantsnssv18154729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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