A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600549



Internal ID20973620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12539644..12593555hg38UCSC Ensembl
chr7:12579270..12633180hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3853912
hg1953911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223150
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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