A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014909



Internal ID19104126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236585945..236642262hg38UCSC Ensembl
Innerchr2:237494588..237550905hg19UCSC Ensembl
Innerchr2:237159327..237215644hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3856318
hg1956318
hg1856318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586955
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)nsv1014909
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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