A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1603



Internal ID15199480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73898881..73943392hg38UCSC Ensembl
Outerchr15:74191222..74235733hg19UCSC Ensembl
Outerchr15:71978275..72022786hg18UCSC Ensembl
Outerchr15:71978275..72022786hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3844512
hg1944512
hg1844512
hg1744512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4636
SamplesNA19129
Known GenesLOXL1, LOXL1-AS1
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)nsv1603
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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