A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428679



Internal ID21086232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155234743..155283367hg38UCSC Ensembl
chr7:155026453..155075077hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3848625
hg1948625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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