A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1877



Internal ID15199754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93782200..93827352hg38UCSC Ensembl
Outerchr1:94247756..94292908hg19UCSC Ensembl
Outerchr1:94020344..94065496hg18UCSC Ensembl
Outerchr1:93959777..94004929hg17UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3845153
hg1945153
hg1845153
hg1745153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4403
SamplesNA12878
Known GenesBCAR3
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)nsv1877
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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