A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751



Internal ID15538479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:124099068..124109171hg38UCSC Ensembl
Outerchr9:126861347..126871450hg19UCSC Ensembl
Outerchr9:125901168..125911271hg18UCSC Ensembl
Outerchr9:123940901..123951004hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386248
hg196248
hg186248
hg176248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6710
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)nssv3751
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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