A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10905



Internal ID15539493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:58326893..58352528hg38UCSC Ensembl
Outerchr12:58720676..58746311hg19UCSC Ensembl
Outerchr12:57006943..57032578hg18UCSC Ensembl
Outerchr12:57006943..57032578hg17UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3825636
hg1925636
hg1825636
hg1725636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv730
Supporting Variants
SamplesNA15510
Known Genes
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)nssv10905
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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