A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440919



Internal ID22107097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88947708..88947846hg38UCSC Ensembl
chr6:89657427..89657565hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762766
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440919
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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