A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965



Internal ID15538692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:22389071..22409428hg38UCSC Ensembl
Outerchr1:22715564..22735921hg19UCSC Ensembl
Outerchr1:22588151..22608508hg18UCSC Ensembl
Outerchr1:22460870..22481227hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3820358
hg1920358
hg1820358
hg1720358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6187
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)nssv3965
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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