A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7086



Internal ID15536778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156551568..156560226hg38UCSC Ensembl
Outerchr1:156521360..156530018hg19UCSC Ensembl
Outerchr1:154787984..154796642hg18UCSC Ensembl
Outerchr1:153334433..153343091hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg388659
hg198659
hg188659
hg178659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3077
Supporting Variants
SamplesNA12156
Known GenesIQGAP3
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)nssv7086
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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