A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668



Internal ID15198511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102526970..102645216hg38UCSC Ensembl
Outerchr7:102167417..102285663hg19UCSC Ensembl
Outerchr7:101954422..102072899hg18UCSC Ensembl
Outerchr7:101761137..101879614hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38118247
hg19118247
hg18118478
hg17118478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879
Supporting Variants
SamplesNA19240
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)nssv668
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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