A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1663



Internal ID15546226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:91266402..91310897hg38UCSC Ensembl
Outerchr15:91809632..91854127hg19UCSC Ensembl
Outerchr15:89610636..89655131hg18UCSC Ensembl
Outerchr15:89610636..89655131hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3844496
hg1944496
hg1844496
hg1744496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4172
SamplesNA12878
Known GenesSV2B
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)nsv1663
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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