A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11141



Internal ID15539438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:4578600..4601638hg38UCSC Ensembl
Outerchr7:4618231..4641269hg19UCSC Ensembl
Outerchr7:4584757..4607795hg18UCSC Ensembl
Outerchr7:4391472..4414510hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3823039
hg1923039
hg1823039
hg1723039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5625
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)nssv11141
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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