A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1983



Internal ID15541266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24811027..24830733hg38UCSC Ensembl
Outerchr1:25137518..25157224hg19UCSC Ensembl
Outerchr1:25010105..25029811hg18UCSC Ensembl
Outerchr1:24882824..24902530hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3819707
hg1919707
hg1819707
hg1719707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7076
Supporting Variants
SamplesNA18555
Known GenesCLIC4
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)nssv1983
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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