A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475163



Internal ID21132716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18043801..18045200hg38UCSC Ensembl
chr12:18196735..18198134hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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