A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464646



Internal ID21122199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94355678..94358881hg38UCSC Ensembl
chr12:94749454..94752657hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383204
hg193204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005401
Samples
Known GenesCCDC41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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