A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141755



Internal ID20708795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36472067..36473255hg38UCSC Ensembl
chr6:36439844..36441032hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412903
Supporting Variants
Samples
Known GenesKCTD20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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