A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1225



Internal ID15544503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105862461..105930543hg38UCSC Ensembl
Outerchr14:106328671..106396403hg19UCSC Ensembl
Outerchr14:105399716..105467448hg18UCSC Ensembl
Outerchr14:105399716..105467448hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3868083
hg1967733
hg1867733
hg1767733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA19240
Known GenesKIAA0125
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)nssv1225
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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