A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461771



Internal ID21119324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69711930..69718042hg38UCSC Ensembl
chr12:70105710..70111822hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg386113
hg196113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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