A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1449



Internal ID15197571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35359290..35412213hg38UCSC Ensembl
Outerchr19:35850192..35903115hg19UCSC Ensembl
Outerchr19:40542032..40594955hg18UCSC Ensembl
Outerchr19:40542032..40594955hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852924
hg1952924
hg1852924
hg1752924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2471
Supporting Variants
SamplesNA19240
Known GenesFFAR3, LOC100128682
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)nssv1449
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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