A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060476



Internal ID19149695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7253529..7300032hg38UCSC Ensembl
Innerchr19:7253540..7300043hg19UCSC Ensembl
Innerchr19:7204540..7251043hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3846504
hg1946504
hg1846504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564671
Samples
Known GenesINSR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060476
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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