A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441597



Internal ID22107778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17722260..17722260hg38UCSC Ensembl
chr19:17833069..17833069hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762062
Samples
Known GenesMAP1S
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441597
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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