A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331472



Internal ID20864635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214296739..214296788hg38UCSC Ensembl
chr1:214470082..214470131hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057802
Samples
Known GenesSMYD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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