A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4396



Internal ID15549101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:78014193..78059551hg38UCSC Ensembl
Outerchr4:78935347..78980705hg19UCSC Ensembl
Outerchr4:79154371..79199729hg18UCSC Ensembl
Outerchr4:79292526..79337884hg17UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3845359
hg1945359
hg1845359
hg1745359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7099
SamplesNA12156
Known GenesFRAS1
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)nsv4396
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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