A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360359



Internal ID21017912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15493306..15500296hg38UCSC Ensembl
chr3:15534813..15541803hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386991
hg196991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096391
Samples
Known GenesCOLQ, MIR4270
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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