A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4646



Internal ID15196599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35167061..35211662hg38UCSC Ensembl
Outerchr19:35657964..35702565hg19UCSC Ensembl
Outerchr19:40349804..40394405hg18UCSC Ensembl
Outerchr19:40349804..40394405hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3844602
hg1944602
hg1844602
hg1744602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2470
Supporting Variants
SamplesNA19129
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)nssv4646
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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