A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3046957



Internal ID21179003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683760..24683760hg38UCSC Ensembl
chr6:24683988..24683988hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14022059
SamplesNA12878
Known GenesACOT13
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)nsv3046957
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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