A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2575



Internal ID15193856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24801738..24818809hg38UCSC Ensembl
Outerchr6:24801966..24819037hg19UCSC Ensembl
Outerchr6:24909945..24927016hg18UCSC Ensembl
Outerchr6:24909945..24927016hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3817072
hg1917072
hg1817072
hg1717072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5227
Supporting Variants
SamplesNA18555
Known GenesFAM65B
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)nssv2575
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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