A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615057



Internal ID20988128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112978294..113077978hg38UCSC Ensembl
chr7:112618349..112718033hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3899685
hg1999685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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