A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv875432



Internal ID6282443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:175590459..175645837hg19UCSC Ensembl
Outerchr2:175585616..175685429hg19UCSC Ensembl
Innerchr2:175298705..175354083hg18UCSC Ensembl
Outerchr2:175293862..175393675hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1585729, nssv1555032
SamplesIS37639, MS21163
Known GenesCHN1, CHRNA1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv875432
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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