A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10935



Internal ID15539523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:72269308..72357511hg38UCSC Ensembl
Outerchr1:72734991..72823194hg19UCSC Ensembl
Outerchr1:72507579..72595782hg18UCSC Ensembl
Outerchr1:72447012..72535215hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3888204
hg1988204
hg1888204
hg1788204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1376
Supporting Variants
SamplesNA15510
Known GenesNEGR1
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)nssv10935
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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