A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218916



Internal ID20785956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74403144..74439548hg38UCSC Ensembl
chr7:73817474..73853878hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3836405
hg1936405
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603604
Supporting Variants
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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