A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445701



Internal ID21103254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7362370..7529664hg38UCSC Ensembl
chr10:7404332..7571626hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38167295
hg19167295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189457
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445701
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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