A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438943



Internal ID22105120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:993957..993957hg38UCSC Ensembl
chr6:994192..994192hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767497
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438943
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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