A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614580



Internal ID20987651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28165369..28167534hg38UCSC Ensembl
chr7:28204988..28207153hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg382166
hg192166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230342
Samples
Known GenesJAZF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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