A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469771



Internal ID21127324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31356402..31367671hg38UCSC Ensembl
chr12:31509336..31520605hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3811270
hg1911270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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