A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6787



Internal ID15190391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:40374069..40429894hg19UCSC Ensembl
Outerchr19:45065909..45121734hg18UCSC Ensembl
Outerchr19:45065909..45121734hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg1955826
hg1855826
hg1755826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2483
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)nssv6787
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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