A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373199



Internal ID21030752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112263501..112264700hg38UCSC Ensembl
chr3:111982348..111983547hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092128
Samples
Known GenesSLC9C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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