A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356239



Internal ID21013792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156065494..156175900hg38UCSC Ensembl
chr3:155783283..155893689hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38110407
hg19110407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096463
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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