A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892



Internal ID15550747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:106318714..106339608hg38UCSC Ensembl
Outerchr7:105959160..105980054hg19UCSC Ensembl
Outerchr7:105746396..105767290hg18UCSC Ensembl
Outerchr7:105553111..105574005hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg386154
hg196154
hg186154
hg176154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5013, nssv673
SamplesNA19240, NA19129
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)nsv5892
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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