A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607620



Internal ID20980691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124212866..124423794hg38UCSC Ensembl
chr7:123852920..124063848hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38210929
hg19210929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7103n223
Supporting Variantsnssv18217575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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