A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762396



Internal ID22096896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15149047..15149047hg38UCSC Ensembl
chr10:15191046..15191046hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448555
Supporting Variants
Samples
Known GenesNMT2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762396
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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