A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1435



Internal ID15197586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10814223..10848907hg38UCSC Ensembl
Outerchr19:10924899..10959583hg19UCSC Ensembl
Outerchr19:10785899..10820583hg18UCSC Ensembl
Outerchr19:10785899..10820583hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386310
hg196310
hg186310
hg176310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2416
Supporting Variants
SamplesNA19240
Known GenesC19orf38, DNM2, MIR199A1, MIR6793, TMED1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv1435
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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