A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578613



Internal ID16019336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11173352..11216950hg38UCSC Ensembl
Innerchr19:11284028..11327626hg19UCSC Ensembl
Innerchr19:11145028..11188626hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3843599
hg1943599
hg1843599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893547
Samples
Known GenesDOCK6, KANK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578613
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer