A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615893



Internal ID20988964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112677851..112723718hg38UCSC Ensembl
chr7:112317906..112363773hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845868
hg1945868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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