A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458632



Internal ID21116185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4157937..4159670hg38UCSC Ensembl
chr12:4267103..4268836hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg381734
hg191734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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