A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096468



Internal ID20663508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156152189..156153974hg38UCSC Ensembl
chr3:155869978..155871763hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362191
Supporting Variants
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096468
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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