A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425614



Internal ID21083167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129126201..129128100hg38UCSC Ensembl
chr7:128766255..128768154hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217740
Samples
Known GenesLOC407835
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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