A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277933



Internal ID20487151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6816549..6816610hg38UCSC Ensembl
chr10:6858511..6858572hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741868
Supporting Variants
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277933
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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