A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371896



Internal ID21029449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112195241..112195796hg38UCSC Ensembl
chr3:111914088..111914643hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092121
Samples
Known GenesSLC9C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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