A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277401



Internal ID20486619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118969988..118969988hg38UCSC Ensembl
chr6:119291153..119291153hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38n/a
hg19n/a
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variants
Supporting Variants
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277401
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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