A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468257



Internal ID21125810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16075091..16102275hg38UCSC Ensembl
chr12:16228025..16255209hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3827185
hg1927185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997665
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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