A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188376



Internal ID20755416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7025880..7048877hg38UCSC Ensembl
chr12:7133184..7156181hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3822998
hg1922998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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