A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4707



Internal ID15542977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:193150641..193169814hg38UCSC Ensembl
Outerchr3:192868430..192887603hg19UCSC Ensembl
Outerchr3:194351124..194370297hg18UCSC Ensembl
Outerchr3:194351132..194370305hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3819174
hg1919174
hg1819174
hg1719174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4174
Supporting Variants
SamplesNA19129
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)nssv4707
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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