A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066617



Internal ID19155836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46190144..46279349hg38UCSC Ensembl
Innerchr19:46693401..46782606hg19UCSC Ensembl
Innerchr19:51385241..51474446hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3889206
hg1989206
hg1889206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3607n100
Supporting Variantsnssv3724901
Samples
Known GenesDKFZp434J0226, IGFL1, RNU6-66P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066617
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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