A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9897



Internal ID15539976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:147683624..147726094hg38UCSC Ensembl
Outerchr6:148004760..148047230hg19UCSC Ensembl
Outerchr6:148046453..148088923hg18UCSC Ensembl
Outerchr6:148046453..148088923hg17UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3842471
hg1942471
hg1842471
hg1742471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525
Supporting Variants
SamplesNA18507
Known Genes
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)nssv9897
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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