A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438781



Internal ID22104958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51735687..51735687hg38UCSC Ensembl
chr10:53495447..53495447hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757010
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438781
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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