A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3863



Internal ID15548515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:68671770..68719913hg38UCSC Ensembl
Outerchr3:68720921..68769064hg19UCSC Ensembl
Outerchr3:68803611..68851754hg18UCSC Ensembl
Outerchr3:68803611..68851754hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3848144
hg1948144
hg1848144
hg1748144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9620, nssv11062, nssv307, nssv2400, nssv5973, nssv3173, nssv10348
SamplesNA18507, NA12878, NA18956, NA15510, NA18555, NA19240, 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)nsv3863
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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