A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459582



Internal ID21117135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32520583..32528537hg38UCSC Ensembl
chr12:32673517..32681471hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg387955
hg197955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000767
Samples
Known GenesFGD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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