A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437256



Internal ID21094809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42961462..43027891hg38UCSC Ensembl
chr10:43456910..43523339hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3866430
hg1966430
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177275
Samples
Known GenesMIR5100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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