A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641



Internal ID15538369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39372183..39532126hg38UCSC Ensembl
Outerchr8:39229702..39389645hg19UCSC Ensembl
Outerchr8:39348859..39508802hg18UCSC Ensembl
Outerchr8:39348859..39508802hg17UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38159944
hg19159944
hg18159944
hg17159944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6163
Supporting Variants
SamplesNA12878
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)nssv3641
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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