A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271207



Internal ID20480425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63488530..63488530hg38UCSC Ensembl
chr17:61565891..61565891hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754405
Supporting Variants
Samples
Known GenesACE
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271207
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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