A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4364



Internal ID15549066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:65938669..65983926hg38UCSC Ensembl
Outerchr4:66804387..66849644hg19UCSC Ensembl
Outerchr4:66486982..66532239hg18UCSC Ensembl
Outerchr4:66633153..66678410hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3845258
hg1945258
hg1845258
hg1745258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7965
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)nsv4364
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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