A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv915009



Internal ID6276936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37260601..37282036hg19UCSC Ensembl
Outerchr22:37259359..37296129hg19UCSC Ensembl
Innerchr22:35590547..35611982hg18UCSC Ensembl
Outerchr22:35589305..35626075hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1557382, nssv1544805, nssv1535357
SamplesMS22644, MS12170, MS16506
Known GenesNCF4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv915009
Frequency
Sample Size6533
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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