A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461842



Internal ID21119395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26252854..26253385hg38UCSC Ensembl
chr12:26405787..26406318hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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