A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460318



Internal ID21117871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7346707..7349133hg38UCSC Ensembl
chr12:7499303..7501729hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg382427
hg192427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460318
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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