A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474089



Internal ID21131642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6801932..6802360hg38UCSC Ensembl
chr12:6911098..6911526hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002680
Samples
Known GenesCD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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