A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012797



Internal ID19102014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:101574038..101685539hg38UCSC Ensembl
Innerchr2:102190500..102302001hg19UCSC Ensembl
Innerchr2:101556932..101668433hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38111502
hg19111502
hg18111502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729171
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012797
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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