A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7847



Internal ID15536017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:111203182..111248397hg38UCSC Ensembl
Outerchr3:110922029..110967244hg19UCSC Ensembl
Outerchr3:112404719..112449934hg18UCSC Ensembl
Outerchr3:112404719..112449934hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3845216
hg1945216
hg1845216
hg1745216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945
Supporting Variants
SamplesNA12156
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)nssv7847
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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