A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6471



Internal ID15537393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26129396..26142334hg38UCSC Ensembl
Outerchr1:26455887..26468825hg19UCSC Ensembl
Outerchr1:26328474..26341412hg18UCSC Ensembl
Outerchr1:26140029..26152967hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812939
hg1912939
hg1812939
hg1712939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7512
Supporting Variants
SamplesNA12156
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)nssv6471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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