A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760776



Internal ID22095264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121584336..121584336hg38UCSC Ensembl
chr10:123343850..123343850hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444501
Supporting Variants
Samples
Known GenesFGFR2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760776
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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