A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6202



Internal ID15204402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:56565012..56600948hg38UCSC Ensembl
Outerchr8:57477571..57513507hg19UCSC Ensembl
Outerchr8:57640125..57676061hg18UCSC Ensembl
Outerchr8:57640125..57676061hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3835937
hg1935937
hg1835937
hg1735937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8496
SamplesNA12156
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)nsv6202
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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