A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748832



Internal ID21387469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156153721..156158805hg38UCSC Ensembl
chr3:155871510..155876594hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg385085
hg195085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433915
Supporting Variants
SamplesMDQ045
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748832
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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