A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8441



Internal ID15188737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:142807761..142831404hg38UCSC Ensembl
Outerchr7:142505445..142529175hg19UCSC Ensembl
Outerchr7:142215572..142239297hg18UCSC Ensembl
Outerchr7:142022287..142046012hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3823644
hg1923731
hg1823726
hg1723726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982
Supporting Variants
SamplesNA12156
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)nssv8441
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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