A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4897



Internal ID15196275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:22155840..22193155hg38UCSC Ensembl
Outerchr6:22156069..22193384hg19UCSC Ensembl
Outerchr6:22264048..22301363hg18UCSC Ensembl
Outerchr6:22264048..22301363hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3837316
hg1937316
hg1837316
hg1737316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5223
Supporting Variants
SamplesNA19129
Known GenesCASC15
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)nssv4897
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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