A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011965



Internal ID19101183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:105898005..105930292hg38UCSC Ensembl
Innerchr2:106514461..106546748hg19UCSC Ensembl
Innerchr2:105880893..105913180hg18UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg3832288
hg1932288
hg1832288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4033n100
Supporting Variantsnssv3580111
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)nsv1011965
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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