A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463199



Internal ID21120752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29348836..29349271hg38UCSC Ensembl
chr12:29501769..29502204hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998577
Samples
Known GenesERGIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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