A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451738



Internal ID21109291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118464223..118464420hg38UCSC Ensembl
chr10:120223735..120223932hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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