A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188



Internal ID15547772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:159665342..159706392hg38UCSC Ensembl
Outerchr1:159635132..159676182hg19UCSC Ensembl
Outerchr1:157901756..157942806hg18UCSC Ensembl
Outerchr1:156448205..156489255hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3841051
hg1941051
hg1841051
hg1741051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7732
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)nsv3188
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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