A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7670



Internal ID15189508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:31952141..31996857hg38UCSC Ensembl
Outerchr20:30539944..30584660hg19UCSC Ensembl
Outerchr20:30003605..30048321hg18UCSC Ensembl
Outerchr20:30003605..30048321hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3844717
hg1944717
hg1844717
hg1744717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3348
Supporting Variants
SamplesNA12156
Known GenesXKR7
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)nssv7670
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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