A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4219



Internal ID15548906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:7671246..7693073hg38UCSC Ensembl
Outerchr4:7672973..7694800hg19UCSC Ensembl
Outerchr4:7723873..7745700hg18UCSC Ensembl
Outerchr4:7791044..7812871hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3821828
hg1921828
hg1821828
hg1721828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7922
SamplesNA12156
Known GenesSORCS2
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)nsv4219
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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