A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061799



Internal ID18804330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11149372..11232027hg38UCSC Ensembl
Innerchr19:11260048..11342703hg19UCSC Ensembl
Innerchr19:11121048..11203703hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3882656
hg1982656
hg1882656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3427n100
Supporting Variantsnssv3723283, nssv3564691, nssv3723282
Samples
Known GenesDOCK6, KANK2, SPC24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061799
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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