A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444296



Internal ID21101849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29606055..29606852hg38UCSC Ensembl
chr10:29894984..29895781hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981360
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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