A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235345



Internal ID20802385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37282034..37282388hg38UCSC Ensembl
chr7:37321638..37321992hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608224
Supporting Variants
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235345
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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