A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006035



Internal ID19095253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34456427..34515720hg38UCSC Ensembl
Innerchr2:34681494..34740787hg19UCSC Ensembl
Innerchr2:34534998..34594291hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3859294
hg1959294
hg1859294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3761n100
Supporting Variantsnssv3575078, nssv3728082
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)nsv1006035
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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