A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7019



Internal ID15536845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:102494292..102538789hg38UCSC Ensembl
Outerchr3:102213136..102257633hg19UCSC Ensembl
Outerchr3:103695826..103740323hg18UCSC Ensembl
Outerchr3:103695826..103740323hg17UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3844498
hg1944498
hg1844498
hg1744498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926
Supporting Variants
SamplesNA12156
Known Genes
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)nssv7019
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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