A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4069



Internal ID15548741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:152140630..152172869hg38UCSC Ensembl
Outerchr3:151858419..151890658hg19UCSC Ensembl
Outerchr3:153341109..153373348hg18UCSC Ensembl
Outerchr3:153341117..153373356hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg387780
hg197780
hg187780
hg177780
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2425
SamplesNA18555
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)nsv4069
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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