A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4909



Internal ID15196255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32028238..32040707hg38UCSC Ensembl
Outerchr6:31996015..32008484hg19UCSC Ensembl
Outerchr6:32103993..32116463hg18UCSC Ensembl
Outerchr6:32103993..32116463hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826807
hg1926807
hg1826807
hg1726807
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5248
Supporting Variants
SamplesNA19129
Known GenesC4A, C4B, C4B_2, CYP21A2
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)nssv4909
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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