A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461656



Internal ID21119209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90806642..90813349hg38UCSC Ensembl
chr12:91200419..91207126hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg386708
hg196708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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