A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3063897



Internal ID21195427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66061631..66070772hg38UCSC Ensembl
chr9:42450553..42459693hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg389142
hg199141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14035031
SamplesNA12878
Known Genes
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)nsv3063897
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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