A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003155



Internal ID19092372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186709551..186739116hg38UCSC Ensembl
Innerchr3:186427340..186456905hg19UCSC Ensembl
Innerchr3:187910034..187939599hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3829566
hg1929566
hg1829566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5004n100
Supporting Variantsnssv3615026
Samples
Known GenesKNG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003155
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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