A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765778



Internal ID22100258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90797290..90797290hg38UCSC Ensembl
chr14:91263634..91263634hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445604
Supporting Variants
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765778
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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