A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv535



Internal ID15544654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26643664..26686676hg38UCSC Ensembl
Outerchr6:26643892..26686904hg19UCSC Ensembl
Outerchr6:26751871..26794883hg18UCSC Ensembl
Outerchr6:26751871..26794883hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3843013
hg1943013
hg1843013
hg1743013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5231
Supporting Variants
SamplesNA19240
Known GenesZNF322
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)nssv535
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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