A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1642



Internal ID15546205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83542416..83587104hg38UCSC Ensembl
Outerchr15:84211168..84255856hg19UCSC Ensembl
Outerchr15:82002172..82046860hg18UCSC Ensembl
Outerchr15:82002172..82046860hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3844689
hg1944689
hg1844689
hg1744689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7208
SamplesNA12156
Known GenesSH3GL3
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)nsv1642
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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