A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7845



Internal ID15536019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:108987197..109032012hg38UCSC Ensembl
Outerchr3:108706044..108750859hg19UCSC Ensembl
Outerchr3:110188734..110233549hg18UCSC Ensembl
Outerchr3:110188734..110233549hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3844816
hg1944816
hg1844816
hg1744816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938
Supporting Variants
SamplesNA12156
Known GenesMORC1
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)nssv7845
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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