A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447234



Internal ID21104787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100903784..100939395hg38UCSC Ensembl
chr10:102663541..102699152hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3835612
hg1935612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977176
Samples
Known GenesFAM178A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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