A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138981



Internal ID20706021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124744301..124746200hg38UCSC Ensembl
chr6:125065447..125067346hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617401
Supporting Variants
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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