A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7921



Internal ID15535943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:7033785..7078503hg38UCSC Ensembl
Outerchr4:7035512..7080230hg19UCSC Ensembl
Outerchr4:7086413..7131131hg18UCSC Ensembl
Outerchr4:7153584..7198302hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3844719
hg1944719
hg1844719
hg1744719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4217
Supporting Variants
SamplesNA12156
Known GenesCCDC96, GRPEL1, LOC100129931, TADA2B
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)nssv7921
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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