A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7863



Internal ID15189315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:128947999..128992631hg38UCSC Ensembl
Outerchr3:128666842..128711474hg19UCSC Ensembl
Outerchr3:130149532..130194164hg18UCSC Ensembl
Outerchr3:130149540..130194172hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3844633
hg1944633
hg1844633
hg1744633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3996
Supporting Variants
SamplesNA12156
Known GenesKIAA1257
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)nssv7863
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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