A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2877



Internal ID15200754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:152191047..152233114hg38UCSC Ensembl
Outerchr1:152163523..152205590hg19UCSC Ensembl
Outerchr1:150430147..150472214hg18UCSC Ensembl
Outerchr1:148976596..149018663hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389372
hg199372
hg189372
hg179372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3381, nssv2531, nssv11080, nssv7067
SamplesNA12156, NA12878, NA15510, NA18555
Known GenesHRNR
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)nsv2877
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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