A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998396



Internal ID19157932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34439671..34502788hg38UCSC Ensembl
Innerchr2:34664738..34727855hg19UCSC Ensembl
Innerchr2:34518242..34581359hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3863118
hg1963118
hg1863118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3757n100
Supporting Variantsnssv3580996
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)nsv998396
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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