A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457203



Internal ID21114756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70010469..70065964hg38UCSC Ensembl
chr12:70404249..70459744hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3855496
hg1955496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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