A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444585



Internal ID21102138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16226965..16232524hg38UCSC Ensembl
chr10:16268964..16274523hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385560
hg195560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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