A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191201



Internal ID21330061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14568337..14568337hg38UCSC Ensembl
chr10:14610336..14610336hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927188
Supporting Variants
SamplesHG002
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191201
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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