A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356



Internal ID15551257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:114605790..114656309hg38UCSC Ensembl
Outerchr8:115618019..115668538hg19UCSC Ensembl
Outerchr8:115687195..115737714hg18UCSC Ensembl
Outerchr8:115687195..115737714hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3850520
hg1950520
hg1850520
hg1750520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10638, nssv9757
SamplesNA18507, NA18956
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)nsv6356
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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