A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447895



Internal ID21105448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30236195..30272231hg38UCSC Ensembl
chr10:30525124..30561160hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3836037
hg1936037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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