A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6163



Internal ID15551045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39368556..39533370hg38UCSC Ensembl
Outerchr8:39226075..39390889hg19UCSC Ensembl
Outerchr8:39345232..39510046hg18UCSC Ensembl
Outerchr8:39345232..39510046hg17UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38164815
hg19164815
hg18164815
hg17164815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641, nssv6215
SamplesNA12156, NA12878
Known GenesADAM3A, ADAM5
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)nsv6163
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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