A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730763



Internal ID20506677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100458004..100458062hg38UCSC Ensembl
chr6:100905880..100905938hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266819
Samples
Known GenesSIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730763
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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