A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898819



Internal ID22673941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99556758..99557642hg38UCSC Ensembl
chr6:100004634..100005518hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446526
Samples
Known GenesCCNC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898819
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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