A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3532



Internal ID15201465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:172028311..172073211hg38UCSC Ensembl
Outerchr1:171997451..172042351hg19UCSC Ensembl
Outerchr1:170264074..170308974hg18UCSC Ensembl
Outerchr1:168729108..168774008hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3844901
hg1944901
hg1844901
hg1744901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7807
SamplesNA12156
Known GenesDNM3
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)nsv3532
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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