A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435



Internal ID15549144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:97151806..97206783hg38UCSC Ensembl
Outerchr4:98072957..98127934hg19UCSC Ensembl
Outerchr4:98291980..98346957hg18UCSC Ensembl
Outerchr4:98430135..98485112hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg386429
hg196429
hg186429
hg176429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7109, nssv4768
SamplesNA12156, NA19129
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)nsv4435
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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