A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450742



Internal ID21108295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49069970..49070287hg38UCSC Ensembl
chr10:50278015..50278332hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980010
Samples
Known GenesVSTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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