A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7956



Internal ID15535908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:54778331..54812435hg38UCSC Ensembl
Outerchr4:55644497..55678601hg19UCSC Ensembl
Outerchr4:55339254..55373358hg18UCSC Ensembl
Outerchr4:55485425..55519529hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385330
hg195330
hg185330
hg175330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4345
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)nssv7956
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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