A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1684



Internal ID15546247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98351079..98375410hg38UCSC Ensembl
Outerchr15:98894308..98918639hg19UCSC Ensembl
Outerchr15:96711831..96736162hg18UCSC Ensembl
Outerchr15:96711831..96736162hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3824332
hg1924332
hg1824332
hg1724332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7219
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)nsv1684
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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