A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6786



Internal ID15537077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39870116..39884185hg38UCSC Ensembl
Outerchr19:40360756..40374825hg19UCSC Ensembl
Outerchr19:45052596..45066665hg18UCSC Ensembl
Outerchr19:45052596..45066665hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3816202
hg1916202
hg1816202
hg1716202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2484
Supporting Variants
SamplesNA12156
Known GenesFCGBP
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)nssv6786
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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