A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443013



Internal ID21100566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1901302..2127166hg38UCSC Ensembl
chr10:1943496..2169360hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38225865
hg19225865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981058
Samples
Known GenesLINC00700, MIR6072
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443013
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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