A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3063900



Internal ID21195430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67573775..67574249hg38UCSC Ensembl
chr9:45150617..45151089hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38475
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14036936
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)nsv3063900
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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