A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1655



Internal ID15546218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:81065402..81110369hg38UCSC Ensembl
Outerchr1:81531087..81576054hg19UCSC Ensembl
Outerchr1:81303675..81348642hg18UCSC Ensembl
Outerchr1:81243108..81288075hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3844968
hg1944968
hg1844968
hg1744968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7298
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)nsv1655
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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