A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440116



Internal ID21097669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43432298..43438442hg38UCSC Ensembl
chr10:43927746..43933890hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386145
hg196145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981643
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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