A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8322



Internal ID15188856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161353994..161398701hg38UCSC Ensembl
Outerchr6:161775026..161819733hg19UCSC Ensembl
Outerchr6:161695016..161739723hg18UCSC Ensembl
Outerchr6:161745437..161790144hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3844708
hg1944708
hg1844708
hg1744708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577
Supporting Variants
SamplesNA12156
Known GenesPARK2
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)nssv8322
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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