A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275975



Internal ID20485193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121584377..121584377hg38UCSC Ensembl
chr10:123343891..123343891hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755197
Supporting Variants
Samples
Known GenesFGFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275975
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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