A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439346



Internal ID21096899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12044692..12051841hg38UCSC Ensembl
chr10:12086691..12093840hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387150
hg197150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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