A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603628



Internal ID20976699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20781501..20784500hg38UCSC Ensembl
chr7:20821121..20824119hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg383000
hg192999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230100
Samples
Known GenesSP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603628
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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