A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456946



Internal ID21114499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45311413..45322057hg38UCSC Ensembl
chr12:45705196..45715840hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3810645
hg1910645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000388
Samples
Known GenesANO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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