A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922



Internal ID15550780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:118484511..118538775hg38UCSC Ensembl
Outerchr7:118124565..118178829hg19UCSC Ensembl
Outerchr7:117911801..117966065hg18UCSC Ensembl
Outerchr7:117718516..117772780hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3854265
hg1954265
hg1854265
hg1754265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9446
SamplesNA18517
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)nsv5922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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