A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444884



Internal ID21102437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44921746..44922212hg38UCSC Ensembl
chr10:45417194..45417660hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980378
Samples
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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