A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11157



Internal ID15192736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102591526..102696287hg38UCSC Ensembl
Outerchr7:102231973..102336734hg19UCSC Ensembl
Outerchr7:102019041..102123970hg18UCSC Ensembl
Outerchr7:101825756..101930685hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38104762
hg19104762
hg18104930
hg17104930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5879
Supporting Variants
SamplesNA15510
Known GenesPOLR2J2, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B, UPK3BL
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)nssv11157
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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