A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295093



Internal ID20504311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41630941..41642110hg38UCSC Ensembl
chr6:41598679..41609848hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3811170
hg1911170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745631
Supporting Variants
Samples
Known GenesMDFI
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295093
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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