A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9722



Internal ID15193302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102541320..102646345hg38UCSC Ensembl
Outerchr7:102181767..102286792hg19UCSC Ensembl
Outerchr7:101968772..102074028hg18UCSC Ensembl
Outerchr7:101775487..101880743hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38105026
hg19105026
hg18105257
hg17105257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5879
Supporting Variants
SamplesNA18507
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)nssv9722
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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