A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3132



Internal ID15547711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:157366179..157379396hg38UCSC Ensembl
Outerchr1:157335969..157349186hg19UCSC Ensembl
Outerchr1:155602593..155615810hg18UCSC Ensembl
Outerchr1:154149042..154162259hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3813218
hg1913218
hg1813218
hg1713218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7724
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)nsv3132
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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