A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723253



Internal ID18674848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3321667..3369170hg38UCSC Ensembl
Innerchr19:3321665..3369168hg19UCSC Ensembl
Innerchr19:3272665..3320168hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3847504
hg1947504
hg1847504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058546
Supporting Variants
Samples
Known GenesNFIC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723253
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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