A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429084



Internal ID21086637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128136402..128148722hg38UCSC Ensembl
chr7:127776454..127788774hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3812321
hg1912321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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