A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3056862



Internal ID21188742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32031896..32031896hg38UCSC Ensembl
chr10:32320824..32320824hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14022249
SamplesCHM1
Known GenesKIF5B
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)nsv3056862
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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