A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603227



Internal ID20976298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57603498..58029244hg38UCSC Ensembl
chr7:57663204..58054331hg19UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38425747
hg19391128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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