A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765063



Internal ID22099535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93618729..93618729hg38UCSC Ensembl
chr9:96381011..96381011hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443268
Supporting Variants
Samples
Known GenesPHF2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765063
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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