A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369412



Internal ID21026965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112265534..112266205hg38UCSC Ensembl
chr3:111984381..111985052hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092130
Samples
Known GenesSLC9C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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