A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9559



Internal ID15193069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:51628421..51660482hg38UCSC Ensembl
Outerchr19:52131674..52163735hg19UCSC Ensembl
Outerchr19:56823486..56855547hg18UCSC Ensembl
Outerchr19:56823486..56855547hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3832062
hg1932062
hg1832062
hg1732062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2532
Supporting Variants
SamplesNA18507
Known GenesSIGLEC14, SIGLEC5
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)nssv9559
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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