A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4580



Internal ID15549304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:160791908..160826228hg38UCSC Ensembl
Outerchr4:161713060..161747380hg19UCSC Ensembl
Outerchr4:161932510..161966830hg18UCSC Ensembl
Outerchr4:162070665..162104985hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385406
hg195406
hg185406
hg175406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3297
SamplesNA12878
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)nsv4580
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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