A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452176



Internal ID21109729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58817901..58823000hg38UCSC Ensembl
chr10:60577661..60582760hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983167
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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