A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035



Internal ID15545598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:49082089..49126235hg38UCSC Ensembl
Outerchr13:49656225..49700371hg19UCSC Ensembl
Outerchr13:48554226..48598372hg18UCSC Ensembl
Outerchr13:48554226..48598372hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3844147
hg1944147
hg1844147
hg1744147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9121
SamplesNA12156
Known GenesFNDC3A
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)nsv1035
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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