A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7782



Internal ID15536082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:25546808..25591529hg38UCSC Ensembl
Outerchr3:25588299..25633020hg19UCSC Ensembl
Outerchr3:25563303..25608024hg18UCSC Ensembl
Outerchr3:25563303..25608024hg17UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3844722
hg1944722
hg1844722
hg1744722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3735
Supporting Variants
SamplesNA12156
Known GenesRARB
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)nssv7782
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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