A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1497



Internal ID15546060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:38112843..38122173hg38UCSC Ensembl
Outerchr15:38405044..38414374hg19UCSC Ensembl
Outerchr15:36192336..36201666hg18UCSC Ensembl
Outerchr15:36192336..36201666hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385100
hg195100
hg185100
hg175100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4146
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)nsv1497
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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