A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4402



Internal ID15549108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:80964092..80998103hg38UCSC Ensembl
Outerchr4:81885246..81919257hg19UCSC Ensembl
Outerchr4:82104270..82138281hg18UCSC Ensembl
Outerchr4:82242425..82276436hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg385427
hg195427
hg185427
hg175427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7973
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)nsv4402
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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