A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437348



Internal ID21094901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4367835..4372734hg38UCSC Ensembl
chr10:4410027..4414926hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981665
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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