A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006101



Internal ID22067732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40910..68920hg38UCSC Ensembl
Outerchr9:40910..88030hg38UCSC Ensembl
Innerchr9:40910..68920hg19UCSC Ensembl
Outerchr9:40910..88030hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3847121
hg1947121
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154402
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006101
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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