A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3021



Internal ID15200903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155275103..155278531hg38UCSC Ensembl
Outerchr1:155244894..155248322hg19UCSC Ensembl
Outerchr1:153511518..153514946hg18UCSC Ensembl
Outerchr1:152057967..152061395hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3836426
hg1936426
hg1836426
hg1736426
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11114
SamplesNA15510
Known GenesHCN3
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)nsv3021
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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