A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9395



Internal ID15193660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:69594002..69618015hg38UCSC Ensembl
Outerchr4:70459720..70483733hg19UCSC Ensembl
Outerchr4:70494309..70518322hg18UCSC Ensembl
Outerchr4:70640480..70664493hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3824014
hg1924014
hg1824014
hg1724014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4377
Supporting Variants
SamplesNA18517
Known GenesUGT2A1, UGT2A2
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)nssv9395
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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