A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1637



Internal ID15199514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:80991050..81035843hg38UCSC Ensembl
Outerchr15:81283391..81328184hg19UCSC Ensembl
Outerchr15:79070446..79115239hg18UCSC Ensembl
Outerchr15:79070446..79115239hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3844794
hg1944794
hg1844794
hg1744794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7206
SamplesNA12156
Known GenesMESDC1, MIR4514
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)nsv1637
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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