A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461834



Internal ID21119387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15797937..15822424hg38UCSC Ensembl
chr12:15950871..15975358hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3824488
hg1924488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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