A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9515



Internal ID15539799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:72296972..72356411hg38UCSC Ensembl
Outerchr1:72762655..72822094hg19UCSC Ensembl
Outerchr1:72535243..72594682hg18UCSC Ensembl
Outerchr1:72474676..72534115hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3859440
hg1959440
hg1859440
hg1759440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1376
Supporting Variants
SamplesNA18507
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)nssv9515
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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