A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316689



Internal ID20849770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245746769..245824574hg38UCSC Ensembl
chr1:245910071..245987876hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3877806
hg1977806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059791
Samples
Known GenesSMYD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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