A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4093



Internal ID15548768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:162761865..162936799hg38UCSC Ensembl
Outerchr3:162479653..162654587hg19UCSC Ensembl
Outerchr3:163962347..164137281hg18UCSC Ensembl
Outerchr3:163962355..164137289hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38174935
hg19174935
hg18174935
hg17174935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11070, nssv3210, nssv9385, nssv9631, nssv2427
SamplesNA18507, NA12878, NA15510, NA18555, NA18517
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)nsv4093
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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