A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893813



Internal ID6300824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124069521..124127005hg19UCSC Ensembl
Outerchr9:124057682..124135334hg19UCSC Ensembl
Innerchr9:123109342..123166826hg18UCSC Ensembl
Outerchr9:123097503..123175155hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1539203
SamplesMS14258
Known GenesGSN, STOM
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893813
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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