A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278281



Internal ID20487499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36363336..36363336hg38UCSC Ensembl
chr6:36331113..36331113hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750877
Supporting Variants
Samples
Known GenesETV7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278281
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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