A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4577



Internal ID15549300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:160013053..160023940hg38UCSC Ensembl
Outerchr4:160934205..160945092hg19UCSC Ensembl
Outerchr4:161153655..161164542hg18UCSC Ensembl
Outerchr4:161291810..161302697hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385702
hg195702
hg185702
hg175702
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10425
SamplesNA18956
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)nsv4577
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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