A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461873



Internal ID21119426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16052501..16065200hg38UCSC Ensembl
chr12:16205435..16218134hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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