A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146499



Internal ID20713539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78660501..78662400hg38UCSC Ensembl
chr6:79370218..79372117hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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