A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7094



Internal ID15190084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:69578750..69619832hg38UCSC Ensembl
Outerchr4:70444468..70485550hg19UCSC Ensembl
Outerchr4:70479057..70520139hg18UCSC Ensembl
Outerchr4:70625228..70666310hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3841083
hg1941083
hg1841083
hg1741083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4377
Supporting Variants
SamplesNA12156
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)nssv7094
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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