A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7796



Internal ID15536068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:42884731..42929105hg38UCSC Ensembl
Outerchr3:42926223..42970597hg19UCSC Ensembl
Outerchr3:42901227..42945601hg18UCSC Ensembl
Outerchr3:42901227..42945601hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3844375
hg1944375
hg1844375
hg1744375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3783
Supporting Variants
SamplesNA12156
Known GenesZNF662
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)nssv7796
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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