A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222969



Internal ID20790009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7375359..7376420hg38UCSC Ensembl
chr6:7375592..7376653hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381062
hg191062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405169
Supporting Variants
Samples
Known GenesCAGE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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