A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6098



Internal ID15191080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:207523387..207573940hg38UCSC Ensembl
Outerchr1:207696732..207747285hg19UCSC Ensembl
Outerchr1:205763355..205813908hg18UCSC Ensembl
Outerchr1:204085127..204135680hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3850554
hg1950554
hg1850554
hg1750554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4232
Supporting Variants
SamplesNA12156
Known GenesCR1
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)nssv6098
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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