A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137



Internal ID15551016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:29840786..29870700hg38UCSC Ensembl
Outerchr8:29698302..29728216hg19UCSC Ensembl
Outerchr8:29817844..29847758hg18UCSC Ensembl
Outerchr8:29817844..29847758hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3829915
hg1929915
hg1829915
hg1729915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8477
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)nsv6137
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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