A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444903



Internal ID22111083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132622236..132622236hg38UCSC Ensembl
chr10:134435740..134435740hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760353
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444903
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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