A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603



Internal ID15550429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170210979..170238787hg38UCSC Ensembl
Outerchr6:170526213..170547875hg19UCSC Ensembl
Outerchr6:170368138..170389800hg18UCSC Ensembl
Outerchr6:170443845..170465507hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg387143
hg197143
hg187143
hg177143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6107
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)nsv5603
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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