A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001159



Internal ID19090376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118183285..118207284hg38UCSC Ensembl
Innerchr2:118940861..118964860hg19UCSC Ensembl
Innerchr2:118657331..118681330hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3824000
hg1924000
hg1824000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729218
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)nsv1001159
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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