A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443491



Internal ID22109674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87492154..87492154hg38UCSC Ensembl
chr13:88144409..88144409hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757440
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443491
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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