A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5826



Internal ID15550674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:87111186..87145415hg38UCSC Ensembl
Outerchr7:86740502..86774731hg19UCSC Ensembl
Outerchr7:86578438..86612667hg18UCSC Ensembl
Outerchr7:86385153..86419382hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385209
hg195209
hg185209
hg175209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8396
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)nsv5826
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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