A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14037599



Internal ID21159814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41830734..41830734hg38UCSC Ensembl
chr21:43250843..43250843hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3066340
Supporting Variants
SamplesCHM1
Known GenesPRDM15
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)nssv14037599
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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