A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4908



Internal ID15196256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32006912..32049614hg38UCSC Ensembl
Outerchr6:31974689..32017391hg19UCSC Ensembl
Outerchr6:32082667..32125369hg18UCSC Ensembl
Outerchr6:32082667..32125369hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3842703
hg1942703
hg1842703
hg1742703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5247
Supporting Variants
SamplesNA19129
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
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)nssv4908
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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