A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600907



Internal ID20973978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90743201..90746000hg38UCSC Ensembl
chr7:90372516..90375315hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223524
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600907
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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