A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446653



Internal ID22112831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102378887..102378887hg38UCSC Ensembl
chr7:102019334..102019334hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759214
Samples
Known GenesLOC100289561, LOC100630923
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446653
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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