A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv866



Internal ID15552887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:52807295..52845436hg38UCSC Ensembl
Outerchr1:53272967..53311108hg19UCSC Ensembl
Outerchr1:53045555..53083696hg18UCSC Ensembl
Outerchr1:52984988..53023129hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3838142
hg1938142
hg1838142
hg1738142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9134
SamplesNA12156
Known GenesZYG11A, ZYG11B
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)nsv866
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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