A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147384



Internal ID20714424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72134361..72134708hg38UCSC Ensembl
chr6:72844064..72844411hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399320
Supporting Variants
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147384
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00101


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