A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445604



Internal ID22111782
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 StatusM
Merged Variants
Supporting Variantsnssv15765778
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445604
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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