A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7767



Internal ID15189411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:4195647..4240502hg38UCSC Ensembl
Outerchr3:4237331..4282186hg19UCSC Ensembl
Outerchr3:4212331..4257186hg18UCSC Ensembl
Outerchr3:4212331..4257186hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3844856
hg1944856
hg1844856
hg1744856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3681
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)nssv7767
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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