A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007759



Internal ID22069390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121678729..121782266hg38UCSC Ensembl
Outerchr9:121676453..121788540hg38UCSC Ensembl
Innerchr9:124441008..124544545hg19UCSC Ensembl
Outerchr9:124438732..124550819hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38112088
hg19112088
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154535
Supporting Variants
Samples
Known GenesDAB2IP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007759
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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