A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9875



Internal ID15539950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:157600677..157629866hg38UCSC Ensembl
Outerchr3:157318466..157347655hg19UCSC Ensembl
Outerchr3:158801160..158830349hg18UCSC Ensembl
Outerchr3:158801168..158830357hg17UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3829190
hg1929190
hg1829190
hg1729190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4081
Supporting Variants
SamplesNA18507
Known GenesC3orf55
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)nssv9875
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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