A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437653



Internal ID22103833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2304291..2304291hg38UCSC Ensembl
chr17:2207585..2207585hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761942
Samples
Known GenesSRR
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437653
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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