A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228519



Internal ID20795559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36444326..36462654hg38UCSC Ensembl
chr7:36483935..36502263hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3818329
hg1918329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602302
Supporting Variants
Samples
Known GenesANLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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