A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3334



Internal ID15191376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:9617788..9626168hg38UCSC Ensembl
Outerchr1:9677846..9686226hg19UCSC Ensembl
Outerchr1:9600433..9608813hg18UCSC Ensembl
Outerchr1:9612112..9620492hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg386346
hg196346
hg186346
hg176346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2187
Supporting Variants
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)nssv3334
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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