A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442609



Internal ID21100162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104755904..104756257hg38UCSC Ensembl
chr10:106515662..106516015hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977767
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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