A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931



Internal ID15548590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:106334002..106368267hg38UCSC Ensembl
Outerchr3:106052849..106087114hg19UCSC Ensembl
Outerchr3:107535539..107569804hg18UCSC Ensembl
Outerchr3:107535539..107569804hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg386731
hg196731
hg186731
hg176731
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv315
SamplesNA19240
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)nsv3931
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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