A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14025164



Internal ID21174439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108991550..108991550hg38UCSC Ensembl
chr13:109643898..109643898hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3057075
Supporting Variants
SamplesNA12878
Known GenesMYO16
MethodSequencing
AnalysisCombines the NGS (e.g., Illumina) and SMS (e.g., Pacbio) for detecting large and small SVs (parameters the same as commit eee31f6 of https://bitbucket.org/xianfan/hybridassemblysv)
Platform
Comments
ReferenceFan_et_al_2017
Pubmed ID28104618
Accession Number(s)nssv14025164
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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