A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3967



Internal ID15201943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:120138861..120184268hg38UCSC Ensembl
Outerchr3:119857708..119903115hg19UCSC Ensembl
Outerchr3:121340398..121385805hg18UCSC Ensembl
Outerchr3:121340398..121385805hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3845408
hg1945408
hg1845408
hg1745408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7026
SamplesNA12156
Known GenesGPR156
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)nsv3967
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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