A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942



Internal ID15204116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:127624959..127655492hg38UCSC Ensembl
Outerchr7:127265013..127295546hg19UCSC Ensembl
Outerchr7:127052249..127082782hg18UCSC Ensembl
Outerchr7:126858964..126889497hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg388904
hg198904
hg188904
hg178904
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6168
SamplesNA12156
Known GenesSND1
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)nsv5942
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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