A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4302



Internal ID15202312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:37289937..37322309hg38UCSC Ensembl
Outerchr4:37291559..37323931hg19UCSC Ensembl
Outerchr4:36967954..37000326hg18UCSC Ensembl
Outerchr4:37114125..37146497hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386860
hg196860
hg186860
hg176860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4735
SamplesNA19129
Known GenesKIAA1239
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)nsv4302
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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