A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467014



Internal ID21124567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83599519..83600924hg38UCSC Ensembl
chr12:83993298..83994703hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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