A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11151



Internal ID15539428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91388391..91416419hg38UCSC Ensembl
Outerchr7:91017706..91045734hg19UCSC Ensembl
Outerchr7:90855642..90883670hg18UCSC Ensembl
Outerchr7:90662357..90690385hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3828029
hg1928029
hg1828029
hg1728029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5834
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11151
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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