A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014911



Internal ID19104128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9723840..9765830hg38UCSC Ensembl
Innerchr2:9863969..9905959hg19UCSC Ensembl
Innerchr2:9781420..9823410hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3841991
hg1941991
hg1841991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576952
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)nsv1014911
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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