A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696212



Internal ID15432864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121676453..121754311hg38UCSC Ensembl
Innerchr9:124438732..124516590hg19UCSC Ensembl
Innerchr9:123478553..123556411hg18UCSC Ensembl
Innerchr9:121518286..121596144hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3877859
hg1977859
hg1877859
hg1777859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518762
Supporting Variants
Samples
Known GenesDAB2IP, MIR548AA1, MIR548D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696212
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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