A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147649



Internal ID20714689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9967401..9972000hg38UCSC Ensembl
chr6:9967634..9972233hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02515


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