A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3064532



Internal ID21196019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112988847..112988847hg38UCSC Ensembl
chr13:113643161..113643161hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14034122
SamplesNA12878
Known GenesMCF2L
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)nsv3064532
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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