A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472070



Internal ID21129623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29354301..29355700hg38UCSC Ensembl
chr12:29507234..29508633hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998578
Samples
Known GenesERGIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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