A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138315



Internal ID20705355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13694624..13695373hg38UCSC Ensembl
chr6:13694856..13695605hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398862
Supporting Variants
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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