A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv871360



Internal ID6278371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7998963..8223832hg19UCSC Ensembl
Outerchr1:7973170..8244145hg19UCSC Ensembl
Innerchr1:7921550..8146419hg18UCSC Ensembl
Outerchr1:7895757..8166732hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1558405
SamplesMS23257
Known GenesERRFI1, PARK7, TNFRSF9
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv871360
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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