A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364101



Internal ID21021654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156186523..156197406hg38UCSC Ensembl
chr3:155904312..155915195hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3810884
hg1910884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209753
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364101
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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