A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14025166



Internal ID21159007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30623768..30623768hg38UCSC Ensembl
chr22:31019755..31019755hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3062121
Supporting Variants
SamplesCHM1
Known GenesTCN2
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)nssv14025166
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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