A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3862



Internal ID15548514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:68558861..68604412hg38UCSC Ensembl
Outerchr3:68608012..68653563hg19UCSC Ensembl
Outerchr3:68690702..68736253hg18UCSC Ensembl
Outerchr3:68690702..68736253hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3845552
hg1945552
hg1845552
hg1745552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5972, nssv2399, nssv10347, nssv3172
SamplesNA12878, NA18956, NA18555, NA19129
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)nsv3862
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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