A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602968



Internal ID20976039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93565601..93593800hg38UCSC Ensembl
chr7:93194913..93223112hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3828200
hg1928200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224225
Samples
Known GenesCALCR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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