A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1557



Internal ID15546120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:61356379..61383552hg38UCSC Ensembl
Outerchr15:61648578..61675751hg19UCSC Ensembl
Outerchr15:59435870..59463043hg18UCSC Ensembl
Outerchr15:59435870..59463043hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg387168
hg197168
hg187168
hg177168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4155
SamplesNA12878
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)nsv1557
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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