A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4356



Internal ID15192397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35164378..35175589hg38UCSC Ensembl
Outerchr19:35655281..35666492hg19UCSC Ensembl
Outerchr19:40347121..40358332hg18UCSC Ensembl
Outerchr19:40347121..40358332hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811212
hg1911212
hg1811212
hg1711212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2470
Supporting Variants
SamplesNA12878
Known GenesFXYD5
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)nssv4356
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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