A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447439



Internal ID21104992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74793913..74800931hg38UCSC Ensembl
chr10:76553671..76560689hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg387019
hg197019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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