A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561



Internal ID15550383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:158478529..158504267hg38UCSC Ensembl
Outerchr6:158899561..158925299hg19UCSC Ensembl
Outerchr6:158819549..158845287hg18UCSC Ensembl
Outerchr6:158869970..158895708hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385415
hg195415
hg185415
hg175415
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483
SamplesNA12878
Known GenesTULP4
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)nsv5561
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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