A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322211



Internal ID20855322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245727993..245793182hg38UCSC Ensembl
chr1:245891295..245956484hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3865190
hg1965190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059790
Samples
Known GenesSMYD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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