A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435630



Internal ID21093183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27992701..27998700hg38UCSC Ensembl
chr10:28281630..28287629hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187597
Samples
Known GenesARMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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