A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3046700



Internal ID21178746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64975423..64975423hg38UCSC Ensembl
chr4:65841141..65841141hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14019894
SamplesNA12878
Known GenesLOC401134
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)nsv3046700
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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